Canonical Allele Identifier: CA2361442243

Gene: MYH7B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34977887G= , CM000682.2:g.34977887G=	GRCh38
NC_000020.10:g.33565690G= , CM000682.1:g.33565690G=	GRCh37
NC_000020.9:g.33029351G=	NCBI36
NG_016984.2:g.26987G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262873.13:c.-72-47G= MANE Select	ENSP00000262873.8:n.-72-47G=
ENST00000262873.12:c.-72-47G=	ENSP00000262873.8:n.-72-47G=
ENST00000618182.6:c.52-47G=	ENSP00000483640.3:n.52-47G=
ENST00000673749.1:n.463-47G=
ENST00000262873.11:c.55-47G=	ENSP00000262873.7:n.55-47G=
ENST00000470929.5:n.15-47G=
ENST00000618182.4:c.52-47G=	ENSP00000483640.1:n.52-47G=
NM_020884.4:c.55-47G=	NP_065935.3:n.55-47G=
XM_006723840.2:c.55-47G=	XP_006723903.1:n.55-47G=
XM_011528941.1:c.55-47G=	XP_011527243.1:n.55-47G=
XM_011528942.1:c.55-47G=	XP_011527244.1:n.55-47G=
XM_011528943.1:c.55-47G=	XP_011527245.1:n.55-47G=
XM_011528944.1:c.55-47G=	XP_011527246.1:n.55-47G=
XM_011528950.1:c.55-47G=	XP_011527252.1:n.55-47G=
XM_006723840.3:c.55-47G=	XP_006723903.1:n.55-47G=
XM_011528941.2:c.55-47G=	XP_011527243.1:n.55-47G=
XM_017027986.1:c.55-47G=	XP_016883475.1:n.55-47G=
NM_020884.5:c.55-47G=	NP_065935.3:n.55-47G=
NM_020884.7:c.-72-47G= MANE Select	NP_065935.4:n.-72-47G=