Canonical Allele Identifier: CA2361442242

Gene: MYH7B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34977885T= , CM000682.2:g.34977885T=	GRCh38
NC_000020.10:g.33565688T= , CM000682.1:g.33565688T=	GRCh37
NC_000020.9:g.33029349T=	NCBI36
NG_016984.2:g.26985T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262873.13:c.-72-49T= MANE Select	ENSP00000262873.8:n.-72-49T=
ENST00000262873.12:c.-72-49T=	ENSP00000262873.8:n.-72-49T=
ENST00000618182.6:c.52-49T=	ENSP00000483640.3:n.52-49T=
ENST00000673749.1:n.463-49T=
ENST00000262873.11:c.55-49T=	ENSP00000262873.7:n.55-49T=
ENST00000470929.5:n.15-49T=
ENST00000618182.4:c.52-49T=	ENSP00000483640.1:n.52-49T=
NM_020884.4:c.55-49T=	NP_065935.3:n.55-49T=
XM_006723840.2:c.55-49T=	XP_006723903.1:n.55-49T=
XM_011528941.1:c.55-49T=	XP_011527243.1:n.55-49T=
XM_011528942.1:c.55-49T=	XP_011527244.1:n.55-49T=
XM_011528943.1:c.55-49T=	XP_011527245.1:n.55-49T=
XM_011528944.1:c.55-49T=	XP_011527246.1:n.55-49T=
XM_011528950.1:c.55-49T=	XP_011527252.1:n.55-49T=
XM_006723840.3:c.55-49T=	XP_006723903.1:n.55-49T=
XM_011528941.2:c.55-49T=	XP_011527243.1:n.55-49T=
XM_017027986.1:c.55-49T=	XP_016883475.1:n.55-49T=
NM_020884.5:c.55-49T=	NP_065935.3:n.55-49T=
NM_020884.7:c.-72-49T= MANE Select	NP_065935.4:n.-72-49T=