Canonical Allele Identifier: CA157909104
Gene: CAMK2B HGNC NCBI

Linked Data

dbSNP Id: rs1065358

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44220153G>A , CM000669.2:g.44220153G>A GRCh38
NC_000007.13:g.44259752G>A , CM000669.1:g.44259752G>A GRCh37
NC_000007.12:g.44226277G>A NCBI36
NG_029407.1:g.110479C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000433930.2:c.937C>T
ENST00000470984.6:c.1151C>T ENSP00000514879.1:p.Ser384Phe
ENST00000484972.6:n.1611C>T
ENST00000700233.1:c.1460C>T ENSP00000514871.1:p.Ser487Phe
ENST00000700234.1:c.521C>T
ENST00000700235.1:c.1595C>T ENSP00000514874.1:p.Ser532Phe
ENST00000700236.1:c.911C>T
ENST00000700237.1:c.1151C>T ENSP00000514876.1:p.Ser384Phe
ENST00000700238.1:c.1079C>T ENSP00000514877.1:p.Ser360Phe
ENST00000700239.1:c.1407C>T
ENST00000700240.1:c.1106C>T ENSP00000514880.1:p.Ser369Phe
ENST00000700241.1:c.1540C>T
ENST00000700283.1:c.1420C>T
ENST00000700284.1:c.*1767C>T ENSP00000514917.1:n.*1767C>T
ENST00000700285.1:c.1538C>T ENSP00000514918.1:p.Ser513Phe
ENST00000700286.1:n.2039C>T
ENST00000700287.1:c.1551C>T
ENST00000700288.1:c.1073C>T ENSP00000514920.1:p.Ser358Phe
ENST00000700290.1:c.1076C>T ENSP00000514921.1:p.Ser359Phe
ENST00000700291.1:c.1335C>T ENSP00000514922.1:n.1335C>T
ENST00000395749.7:c.1910C>T MANE Select ENSP00000379098.2:p.Ser637Phe
ENST00000258682.10:c.1463C>T ENSP00000258682.6:p.Ser488Phe
ENST00000346990.8:c.1259C>T ENSP00000326518.5:p.Ser420Phe
ENST00000347193.8:c.1388C>T ENSP00000326544.6:p.Ser463Phe
ENST00000350811.7:c.1538C>T ENSP00000326375.5:p.Ser513Phe
ENST00000353185.7:c.*331C>T ENSP00000326600.4:n.*331C>T
ENST00000353625.8:c.1349C>T ENSP00000326427.5:p.Ser450Phe
ENST00000358707.7:c.1421C>T ENSP00000351542.3:p.Ser474Phe
ENST00000395747.6:c.1466C>T ENSP00000379096.2:p.Ser489Phe
ENST00000395749.6:c.1910C>T ENSP00000379098.2:p.Ser637Phe
ENST00000425809.5:c.464C>T ENSP00000410445.1:p.Ser155Phe
ENST00000440254.6:c.1538C>T ENSP00000397937.2:p.Ser513Phe
ENST00000457475.5:c.1466C>T ENSP00000390292.1:p.Ser489Phe
ENST00000466584.5:n.365C>T
ENST00000489429.5:n.1994C>T
ENST00000497584.5:n.1789C>T
ENST00000523845.5:c.*1193C>T ENSP00000428912.1:n.*1193C>T
NM_001220.4:c.1910C>T NP_001211.3:p.Ser637Phe
NM_001293170.1:c.1538C>T NP_001280099.1:p.Ser513Phe
NM_172078.2:c.1538C>T NP_742075.1:p.Ser513Phe
NM_172079.2:c.1466C>T NP_742076.1:p.Ser489Phe
NM_172080.2:c.1463C>T NP_742077.1:p.Ser488Phe
NM_172081.2:c.1421C>T NP_742078.1:p.Ser474Phe
NM_172082.2:c.1388C>T NP_742079.1:p.Ser463Phe
NM_172083.2:c.1349C>T NP_742080.1:p.Ser450Phe
NM_172084.2:c.1259C>T NP_742081.1:p.Ser420Phe
XM_005249862.3:c.1493C>T XP_005249919.1:p.Ser498Phe
XM_005249864.3:c.1394C>T XP_005249921.1:p.Ser465Phe
XM_006715781.2:c.1790C>T XP_006715844.1:p.Ser597Phe
XM_006715784.2:c.1466C>T XP_006715847.1:p.Ser489Phe
XM_011515547.1:c.2039C>T XP_011513849.1:p.Ser680Phe
XM_011515548.1:c.2039C>T XP_011513850.1:p.Ser680Phe
XM_011515549.1:c.1994C>T XP_011513851.1:p.Ser665Phe
XM_011515550.1:c.1967C>T XP_011513852.1:p.Ser656Phe
XM_011515551.1:c.1967C>T XP_011513853.1:p.Ser656Phe
XM_011515552.1:c.1964C>T XP_011513854.1:p.Ser655Phe
XM_011515553.1:c.1925C>T XP_011513855.1:p.Ser642Phe
XM_011515554.1:c.1919C>T XP_011513856.1:p.Ser640Phe
XM_011515555.1:c.1910C>T XP_011513857.1:p.Ser637Phe
XM_011515556.1:c.1895C>T XP_011513858.1:p.Ser632Phe
XM_011515557.1:c.1892C>T XP_011513859.1:p.Ser631Phe
XM_011515559.1:c.1652C>T XP_011513861.1:p.Ser551Phe
XM_011515560.1:c.1652C>T XP_011513862.1:p.Ser551Phe
XM_011515559.2:c.1652C>T XP_011513861.1:p.Ser551Phe
XM_017012660.1:c.1922C>T XP_016868149.1:p.Ser641Phe
XM_017012661.1:c.1880C>T XP_016868150.1:p.Ser627Phe
XM_017012662.1:c.1721C>T XP_016868151.1:p.Ser574Phe
XM_017012663.2:c.1580C>T XP_016868152.1:p.Ser527Phe
XM_017012664.1:c.1418C>T XP_016868153.1:p.Ser473Phe
XM_017012665.1:c.1391C>T XP_016868154.1:p.Ser464Phe
XM_017012666.2:c.1151C>T XP_016868155.1:p.Ser384Phe
XM_017012667.2:c.1106C>T XP_016868156.1:p.Ser369Phe
XM_017012668.2:c.1079C>T XP_016868157.1:p.Ser360Phe
XM_017012669.2:c.1079C>T XP_016868158.1:p.Ser360Phe
XM_017012670.2:c.1034C>T XP_016868159.1:p.Ser345Phe
XM_024446945.1:c.1796C>T XP_024302713.1:p.Ser599Phe
XM_024446946.1:c.1076C>T XP_024302714.1:p.Ser359Phe
NM_001220.5:c.1910C>T MANE Select NP_001211.3:p.Ser637Phe
NM_001293170.2:c.1538C>T NP_001280099.1:p.Ser513Phe
NM_172078.3:c.1538C>T NP_742075.1:p.Ser513Phe
NM_172080.3:c.1463C>T NP_742077.1:p.Ser488Phe
NM_172081.3:c.1421C>T NP_742078.1:p.Ser474Phe
NM_172082.3:c.1388C>T NP_742079.1:p.Ser463Phe
NM_172083.3:c.1349C>T NP_742080.1:p.Ser450Phe
NM_172084.3:c.1259C>T NP_742081.1:p.Ser420Phe
NM_172079.3:c.1466C>T NP_742076.1:p.Ser489Phe