Canonical Allele Identifier: CA398166644
Gene: MYH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10641147C>A , CM000679.2:g.10641147C>A GRCh38
NC_000017.10:g.10544464C>A , CM000679.1:g.10544464C>A GRCh37
NC_000017.9:g.10485189C>A NCBI36
NG_011537.1:g.21152G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000583535.6:c.2103G>T MANE Select ENSP00000464317.1:p.Glu701Asp
ENST00000583535.5:c.2103G>T ENSP00000464317.1:p.Glu701Asp
NM_002470.3:c.2103G>T NP_002461.2:p.Glu701Asp
XM_011523870.1:c.2103G>T XP_011522172.1:p.Glu701Asp
XM_011523871.1:c.2103G>T XP_011522173.1:p.Glu701Asp
XM_011523872.1:c.2103G>T XP_011522174.1:p.Glu701Asp
XM_011523870.3:c.2103G>T XP_011522172.1:p.Glu701Asp
XM_011523871.2:c.2103G>T XP_011522173.1:p.Glu701Asp
NM_002470.4:c.2103G>T MANE Select NP_002461.2:p.Glu701Asp