Canonical Allele Identifier: CA398156754
Gene: MYH3 HGNC NCBI

Linked Data

dbSNP Id: rs2074249367

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10639597G>A , CM000679.2:g.10639597G>A GRCh38
NC_000017.10:g.10542914G>A , CM000679.1:g.10542914G>A GRCh37
NC_000017.9:g.10483639G>A NCBI36
NG_011537.1:g.22702C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000583535.6:c.2888C>T MANE Select ENSP00000464317.1:p.Ala963Val
ENST00000583535.5:c.2888C>T ENSP00000464317.1:p.Ala963Val
NM_002470.3:c.2888C>T NP_002461.2:p.Ala963Val
XM_011523870.1:c.2888C>T XP_011522172.1:p.Ala963Val
XM_011523871.1:c.2888C>T XP_011522173.1:p.Ala963Val
XM_011523872.1:c.2888C>T XP_011522174.1:p.Ala963Val
XM_011523870.3:c.2888C>T XP_011522172.1:p.Ala963Val
XM_011523871.2:c.2888C>T XP_011522173.1:p.Ala963Val
NM_002470.4:c.2888C>T MANE Select NP_002461.2:p.Ala963Val