Canonical Allele Identifier: CA2361442279

Gene: MYH7B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34977956T= , CM000682.2:g.34977956T=	GRCh38
NC_000020.10:g.33565759T= , CM000682.1:g.33565759T=	GRCh37
NC_000020.9:g.33029420T=	NCBI36
NG_016984.2:g.27056T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262873.13:c.-50T= MANE Select	ENSP00000262873.8:n.-50T=
ENST00000262873.12:c.-50T=	ENSP00000262873.8:n.-50T=
ENST00000618182.6:c.74T=	ENSP00000483640.3:p.Leu25=
ENST00000673749.1:n.485T=
ENST00000262873.11:c.77T=	ENSP00000262873.7:p.Leu26=
ENST00000470929.5:n.37T=
ENST00000618182.4:c.74T=	ENSP00000483640.1:p.Leu25=
NM_020884.4:c.77T=	NP_065935.3:p.Leu26=
XM_006723840.2:c.77T=	XP_006723903.1:p.Leu26=
XM_011528941.1:c.77T=	XP_011527243.1:p.Leu26=
XM_011528942.1:c.77T=	XP_011527244.1:p.Leu26=
XM_011528943.1:c.77T=	XP_011527245.1:p.Leu26=
XM_011528944.1:c.77T=	XP_011527246.1:p.Leu26=
XM_011528945.1:c.-433T=	XP_011527247.1:n.-433T=
XM_011528950.1:c.77T=	XP_011527252.1:p.Leu26=
XM_006723840.3:c.77T=	XP_006723903.1:p.Leu26=
XM_011528941.2:c.77T=	XP_011527243.1:p.Leu26=
XM_017027986.1:c.77T=	XP_016883475.1:p.Leu26=
NM_020884.5:c.77T=	NP_065935.3:p.Leu26=
NM_020884.7:c.-50T= MANE Select	NP_065935.4:n.-50T=