Canonical Allele Identifier: CA398155652
Gene: MYH3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10639371T>C , CM000679.2:g.10639371T>C GRCh38
NC_000017.10:g.10542688T>C , CM000679.1:g.10542688T>C GRCh37
NC_000017.9:g.10483413T>C NCBI36
NG_011537.1:g.22928A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000583535.6:c.3029A>G MANE Select ENSP00000464317.1:p.Asp1010Gly
ENST00000583535.5:c.3029A>G ENSP00000464317.1:p.Asp1010Gly
NM_002470.3:c.3029A>G NP_002461.2:p.Asp1010Gly
XM_011523870.1:c.3029A>G XP_011522172.1:p.Asp1010Gly
XM_011523871.1:c.3029A>G XP_011522173.1:p.Asp1010Gly
XM_011523872.1:c.3029A>G XP_011522174.1:p.Asp1010Gly
XM_011523870.3:c.3029A>G XP_011522172.1:p.Asp1010Gly
XM_011523871.2:c.3029A>G XP_011522173.1:p.Asp1010Gly
NM_002470.4:c.3029A>G MANE Select NP_002461.2:p.Asp1010Gly