Canonical Allele Identifier: CA2247317256

Gene: MYH3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639965A= , CM000679.2:g.10639965A=	GRCh38
NC_000017.10:g.10543282A= , CM000679.1:g.10543282A=	GRCh37
NC_000017.9:g.10484007A=	NCBI36
NG_011537.1:g.22334T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000583535.6:c.2682+31T= MANE Select	ENSP00000464317.1:n.2682+31T=
ENST00000583535.5:c.2682+31T=	ENSP00000464317.1:n.2682+31T=
NM_002470.3:c.2682+31T=	NP_002461.2:n.2682+31T=
XM_011523870.1:c.2682+31T=	XP_011522172.1:n.2682+31T=
XM_011523871.1:c.2682+31T=	XP_011522173.1:n.2682+31T=
XM_011523872.1:c.2682+31T=	XP_011522174.1:n.2682+31T=
XM_011523870.3:c.2682+31T=	XP_011522172.1:n.2682+31T=
XM_011523871.2:c.2682+31T=	XP_011522173.1:n.2682+31T=
NM_002470.4:c.2682+31T= MANE Select	NP_002461.2:n.2682+31T=