Canonical Allele Identifier: CA398127032

Gene: MYH3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10628667C>T , CM000679.2:g.10628667C>T	GRCh38
NC_000017.10:g.10531984C>T , CM000679.1:g.10531984C>T	GRCh37
NC_000017.9:g.10472709C>T	NCBI36
NG_011537.1:g.33632G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002470.4:c.5809G>A MANE Select	NP_002461.2:p.Glu1937Lys
ENST00000583535.6:c.5809G>A MANE Select	ENSP00000464317.1:p.Glu1937Lys
NM_002470.3:c.5809G>A	NP_002461.2:p.Glu1937Lys
ENST00000577963.1:n.351G>A
ENST00000579928.2:n.339G>A
ENST00000583535.5:c.5809G>A	ENSP00000464317.1:p.Glu1937Lys
XM_011523870.1:c.5809G>A	XP_011522172.1:p.Glu1937Lys
XM_011523870.3:c.5809G>A	XP_011522172.1:p.Glu1937Lys
XM_011523871.1:c.5809G>A	XP_011522173.1:p.Glu1937Lys
XM_011523871.2:c.5809G>A	XP_011522173.1:p.Glu1937Lys