Canonical Allele Identifier: CA376071936
Gene: CACNB2 HGNC NCBI
NSUN6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.18539471A>G , CM000672.2:g.18539471A>G GRCh38
NC_000010.10:g.18828400A>G , CM000672.1:g.18828400A>G GRCh37
NC_000010.9:g.18868406A>G NCBI36
NG_016195.1:g.403795A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000377315.6:c.1586A>G (CACNB2) ENSP00000366532.4:p.Asp529Gly
ENST00000377319.9:c.1451A>G (CACNB2) ENSP00000366536.3:p.Asp484Gly
ENST00000645287.2:c.1574A>G (CACNB2) ENSP00000496203.1:p.Asp525Gly
ENST00000282343.13:c.1646A>G (CACNB2) ENSP00000282343.8:p.Asp549Gly
ENST00000324631.13:c.1730A>G (CACNB2) MANE Select ENSP00000320025.8:p.Asp577Gly
ENST00000377315.5:c.1586A>G (CACNB2) ENSP00000366532.4:p.Asp529Gly
ENST00000377319.8:c.1451A>G (CACNB2) ENSP00000366536.3:p.Asp484Gly
ENST00000377329.10:c.1568A>G (CACNB2) MANE Plus Clinical ENSP00000366546.4:p.Asp523Gly
ENST00000377331.8:c.1355A>G (CACNB2) ENSP00000366548.4:p.Asp452Gly
ENST00000643096.2:c.1532A>G (CACNB2) ENSP00000494209.2:p.Asp511Gly
ENST00000645287.1:c.1574A>G (CACNB2) ENSP00000496203.1:p.Asp525Gly
ENST00000647168.2:c.*871A>G (CACNB2) ENSP00000495854.2:n.*871A>G
ENST00000650685.1:c.1472A>G (CACNB2) ENSP00000498460.1:p.Asp491Gly
ENST00000651330.1:c.*1004A>G (CACNB2) ENSP00000498457.1:n.*1004A>G
ENST00000651468.1:c.1287A>G (CACNB2) ENSP00000498352.1:n.1287A>G
ENST00000651928.1:c.*969A>G (CACNB2) ENSP00000499177.1:n.*969A>G
ENST00000652391.1:c.1550A>G (CACNB2) ENSP00000498938.1:p.Asp517Gly
ENST00000652478.1:c.*830A>G (CACNB2) ENSP00000498812.1:n.*830A>G
ENST00000282343.12:c.1646A>G (CACNB2) ENSP00000282343.8:p.Asp549Gly
ENST00000324631.11:c.1730A>G (CACNB2) ENSP00000320025.7:p.Asp577Gly
ENST00000352115.10:c.1658A>G (CACNB2) ENSP00000344474.6:p.Asp553Gly
ENST00000377315.4:c.1586A>G (CACNB2) ENSP00000366532.4:p.Asp529Gly
ENST00000377319.7:c.1451A>G (CACNB2) ENSP00000366536.3:p.Asp484Gly
ENST00000377328.5:c.980A>G (CACNB2) ENSP00000366545.1:p.Asp327Gly
ENST00000377329.8:c.1568A>G (CACNB2) ENSP00000366546.4:p.Asp523Gly
ENST00000377331.6:c.1574A>G (CACNB2) ENSP00000366548.2:p.Asp525Gly
ENST00000396576.6:c.1565A>G (CACNB2) ENSP00000379821.2:p.Asp522Gly
ENST00000612134.4:c.1434A>G (CACNB2) ENSP00000480563.1:n.1434A>G
ENST00000612743.1:c.242A>G (CACNB2) ENSP00000478676.1:p.Asp81Gly
ENST00000615785.4:c.815A>G (CACNB2) ENSP00000480260.1:p.Asp272Gly
ENST00000617363.4:c.1493A>G (CACNB2) ENSP00000479756.1:p.Asp498Gly
NM_000724.3:c.1565A>G (CACNB2) NP_000715.2:p.Asp522Gly
NM_001167945.1:c.1532A>G (CACNB2) NP_001161417.1:p.Asp511Gly
NM_201570.2:c.1586A>G (CACNB2) NP_963864.1:p.Asp529Gly
NM_201571.3:c.1646A>G (CACNB2) NP_963865.2:p.Asp549Gly
NM_201572.3:c.1574A>G (CACNB2) NP_963866.2:p.Asp525Gly
NM_201590.2:c.1568A>G (CACNB2) NP_963884.2:p.Asp523Gly
NM_201593.2:c.1616A>G (CACNB2) NP_963887.2:p.Asp539Gly
NM_201596.2:c.1730A>G (CACNB2) NP_963890.2:p.Asp577Gly
NM_201597.2:c.1658A>G (CACNB2) NP_963891.1:p.Asp553Gly
XM_005252588.2:c.1472A>G (CACNB2) XP_005252645.1:p.Asp491Gly
XM_005252591.2:c.890A>G (CACNB2) XP_005252648.1:p.Asp297Gly
XM_006717502.2:c.1550A>G (CACNB2) XP_006717565.1:p.Asp517Gly
XM_011519659.1:c.1496A>G (CACNB2) XP_011517961.1:p.Asp499Gly
XM_011519660.1:c.1451A>G (CACNB2) XP_011517962.1:p.Asp484Gly
NM_001330060.1:c.1451A>G (CACNB2) NP_001316989.1:p.Asp484Gly
XM_005252588.4:c.1472A>G (CACNB2) XP_005252645.1:p.Asp491Gly
XM_005252591.3:c.890A>G (CACNB2) XP_005252648.1:p.Asp297Gly
XM_006717502.3:c.1550A>G (CACNB2) XP_006717565.1:p.Asp517Gly
XM_011519659.2:c.1496A>G (CACNB2) XP_011517961.1:p.Asp499Gly
XM_017016625.1:c.890A>G (CACNB2) XP_016872114.1:p.Asp297Gly
XR_001747060.1:n.2423+2598T>C (NSUN6)
XR_001747198.1:n.1855A>G (CACNB2)
NM_000724.4:c.1565A>G (CACNB2) NP_000715.2:p.Asp522Gly
NM_001167945.2:c.1532A>G (CACNB2) NP_001161417.1:p.Asp511Gly
NM_001330060.2:c.1451A>G (CACNB2) NP_001316989.1:p.Asp484Gly
NM_201570.3:c.1586A>G (CACNB2) NP_963864.1:p.Asp529Gly
NM_201571.4:c.1646A>G (CACNB2) NP_963865.2:p.Asp549Gly
NM_201572.4:c.1574A>G (CACNB2) NP_963866.2:p.Asp525Gly
NM_201590.3:c.1568A>G (CACNB2) MANE Plus Clinical NP_963884.2:p.Asp523Gly
NM_201593.3:c.1616A>G (CACNB2) NP_963887.2:p.Asp539Gly
NM_201596.3:c.1730A>G (CACNB2) MANE Select NP_963890.2:p.Asp577Gly
NM_201597.3:c.1658A>G (CACNB2) NP_963891.1:p.Asp553Gly