Canonical Allele Identifier: CA123758
Gene: MYH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 14141
ClinVar RCV Id: RCV000015204
dbSNP Id: rs121913620

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10640204A>T , CM000679.2:g.10640204A>T GRCh38
NC_000017.10:g.10543521A>T , CM000679.1:g.10543521A>T GRCh37
NC_000017.9:g.10484246A>T NCBI36
NG_011537.1:g.22095T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000583535.6:c.2474T>A MANE Select ENSP00000464317.1:p.Val825Asp
ENST00000583535.5:c.2474T>A ENSP00000464317.1:p.Val825Asp
NM_002470.3:c.2474T>A NP_002461.2:p.Val825Asp
XM_011523870.1:c.2474T>A XP_011522172.1:p.Val825Asp
XM_011523871.1:c.2474T>A XP_011522173.1:p.Val825Asp
XM_011523872.1:c.2474T>A XP_011522174.1:p.Val825Asp
XM_011523870.3:c.2474T>A XP_011522172.1:p.Val825Asp
XM_011523871.2:c.2474T>A XP_011522173.1:p.Val825Asp
NM_002470.4:c.2474T>A MANE Select NP_002461.2:p.Val825Asp