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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.158685347C>T , CM000663.2:g.158685347C>T
GRCh38
NC_000001.10:g.158655137C>T , CM000663.1:g.158655137C>T
GRCh37
NC_000001.9:g.156921761C>T
NCBI36
NG_011474.1:g.6370G>A
Transcript Alleles
HGVS
Amino-acid Change
ENST00000643759.2:c.25G>A
MANE Select
ENSP00000495214.1:p.Val9Ile
ENST00000368147.8:c.25G>A
ENSP00000357129.4:p.Val9Ile
ENST00000467387.1:c.25G>A
ENSP00000476485.1:p.Val9Ile
ENST00000614909.4:c.25G>A
ENSP00000482595.1:p.Val9Ile
NM_003126.2:c.25G>A
NP_003117.2:p.Val9Ile
XM_011509916.1:c.25G>A
XP_011508218.1:p.Val9Ile
XM_011509917.1:c.25G>A
XP_011508219.1:p.Val9Ile
XM_011509918.1:c.25G>A
XP_011508220.1:p.Val9Ile
XM_011509919.1:c.25G>A
XP_011508221.1:p.Val9Ile
XR_921911.1:n.138G>A
XR_921912.1:n.143G>A
NM_003126.3:c.25G>A
NP_003117.2:p.Val9Ile
XM_011509916.2:c.25G>A
XP_011508218.1:p.Val9Ile
XM_011509917.3:c.25G>A
XP_011508219.1:p.Val9Ile
XM_011509918.3:c.25G>A
XP_011508220.1:p.Val9Ile
XM_011509919.3:c.25G>A
XP_011508221.1:p.Val9Ile
XR_921911.3:n.151G>A
XR_921912.2:n.153G>A
NM_003126.4:c.25G>A
MANE Select
NP_003117.2:p.Val9Ile