Canonical Allele Identifier: CA2361448096

Gene: MYH7B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34989186C= , CM000682.2:g.34989186C=	GRCh38
NC_000020.10:g.33576989C= , CM000682.1:g.33576989C=	GRCh37
NC_000020.9:g.33040650C=	NCBI36
NG_016984.2:g.38286C=

Transcript Alleles

HGVS	Amino-acid Change
NM_020884.7:c.1588-554C= MANE Select	NP_065935.4:n.1588-554C=
ENST00000262873.13:c.1588-554C= MANE Select	ENSP00000262873.8:n.1588-554C=
NM_020884.4:c.1714-554C=	NP_065935.3:n.1714-554C=
NM_020884.5:c.1714-554C=	NP_065935.3:n.1714-554C=
ENST00000262873.11:c.1714-554C=	ENSP00000262873.7:n.1714-554C=
ENST00000262873.12:c.1588-554C=	ENSP00000262873.8:n.1588-554C=
ENST00000618182.4:c.1711-554C=	ENSP00000483640.1:n.1711-554C=
ENST00000618182.6:c.1711-554C=	ENSP00000483640.3:n.1711-554C=
XM_006723840.2:c.1714-554C=	XP_006723903.1:n.1714-554C=
XM_006723840.3:c.1714-554C=	XP_006723903.1:n.1714-554C=
XM_011528941.1:c.1678-138C=	XP_011527243.1:n.1678-138C=
XM_011528941.2:c.1678-138C=	XP_011527243.1:n.1678-138C=
XM_011528942.1:c.1678-138C=	XP_011527244.1:n.1678-138C=
XM_011528943.1:c.1678-554C=	XP_011527245.1:n.1678-554C=
XM_011528944.1:c.1579-138C=	XP_011527246.1:n.1579-138C=
XM_011528945.1:c.1108-138C=	XP_011527247.1:n.1108-138C=
XM_011528946.1:c.1096-138C=	XP_011527248.1:n.1096-138C=
XM_011528947.1:c.901-138C=	XP_011527249.1:n.901-138C=
XM_011528947.2:c.901-138C=	XP_011527249.1:n.901-138C=
XM_011528948.1:c.901-138C=	XP_011527250.1:n.901-138C=
XM_011528948.2:c.901-138C=	XP_011527250.1:n.901-138C=
XM_011528950.1:c.1678-138C=	XP_011527252.1:n.1678-138C=
XM_017027986.1:c.1714-138C=	XP_016883475.1:n.1714-138C=
XR_001754582.1:n.571G=