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Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.96121323C>A , CM000669.2:g.96121323C>A
GRCh38
NC_000007.13:g.95750635C>A , CM000669.1:g.95750635C>A
GRCh37
NC_000007.12:g.95588571C>A
NCBI36
NG_012247.1:g.205825G>T
NG_012247.2:g.205825G>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000265631.10:c.1896G>T
MANE Select
ENSP00000265631.6:p.Pro632=
ENST00000265631.9:c.1896G>T
ENSP00000265631.5:p.Pro632=
ENST00000416240.6:c.1899G>T
ENSP00000400101.2:p.Pro633=
ENST00000494085.1:n.399G>T
NM_001160210.1:c.1899G>T
NP_001153682.1:p.Pro633=
NM_014251.2:c.1896G>T
NP_055066.1:p.Pro632=
NR_027662.1:n.1971G>T
XM_006715831.2:c.1929G>T
XP_006715894.1:p.Pro643=
XM_011515728.1:c.1044G>T
XP_011514030.1:p.Pro348=
XM_006715831.4:c.1929G>T
XP_006715894.1:p.Pro643=
XM_017011663.1:c.1887G>T
XP_016867152.1:p.Pro629=
XM_017011664.2:c.1044G>T
XP_016867153.1:p.Pro348=
XM_017011665.1:c.1044G>T
XP_016867154.1:p.Pro348=
XR_001744525.2:n.2142G>T
XR_002956405.1:n.2700G>T
NM_014251.3:c.1896G>T
MANE Select
NP_055066.1:p.Pro632=
NR_027662.2:n.1922G>T
NM_001160210.2:c.1899G>T
NP_001153682.1:p.Pro633=