Canonical Allele Identifier: CA2247332895

Gene: MYH3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639391C= , CM000679.2:g.10639391C=	GRCh38
NC_000017.10:g.10542708C= , CM000679.1:g.10542708C=	GRCh37
NC_000017.9:g.10483433C=	NCBI36
NG_011537.1:g.22908G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.3009G= MANE Select	ENSP00000464317.1:p.Ala1003=
ENST00000583535.5:c.3009G=	ENSP00000464317.1:p.Ala1003=
NM_002470.3:c.3009G=	NP_002461.2:p.Ala1003=
XM_011523870.1:c.3009G=	XP_011522172.1:p.Ala1003=
XM_011523871.1:c.3009G=	XP_011522173.1:p.Ala1003=
XM_011523872.1:c.3009G=	XP_011522174.1:p.Ala1003=
XM_011523870.3:c.3009G=	XP_011522172.1:p.Ala1003=
XM_011523871.2:c.3009G=	XP_011522173.1:p.Ala1003=
NM_002470.4:c.3009G= MANE Select	NP_002461.2:p.Ala1003=