Canonical Allele Identifier: CA2577378776

Gene: MYH7B

Linked Data

• gnomAD v4: 20-34977888-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34977888G>T , CM000682.2:g.34977888G>T	GRCh38
NC_000020.10:g.33565691G>T , CM000682.1:g.33565691G>T	GRCh37
NC_000020.9:g.33029352G>T	NCBI36
NG_016984.2:g.26988G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262873.13:c.-72-46G>T MANE Select	ENSP00000262873.8:n.-72-46G>T
ENST00000262873.12:c.-72-46G>T	ENSP00000262873.8:n.-72-46G>T
ENST00000618182.6:c.52-46G>T	ENSP00000483640.3:n.52-46G>T
ENST00000673749.1:n.463-46G>T
ENST00000262873.11:c.55-46G>T	ENSP00000262873.7:n.55-46G>T
ENST00000470929.5:n.15-46G>T
ENST00000618182.4:c.52-46G>T	ENSP00000483640.1:n.52-46G>T
NM_020884.4:c.55-46G>T	NP_065935.3:n.55-46G>T
XM_006723840.2:c.55-46G>T	XP_006723903.1:n.55-46G>T
XM_011528941.1:c.55-46G>T	XP_011527243.1:n.55-46G>T
XM_011528942.1:c.55-46G>T	XP_011527244.1:n.55-46G>T
XM_011528943.1:c.55-46G>T	XP_011527245.1:n.55-46G>T
XM_011528944.1:c.55-46G>T	XP_011527246.1:n.55-46G>T
XM_011528950.1:c.55-46G>T	XP_011527252.1:n.55-46G>T
XM_006723840.3:c.55-46G>T	XP_006723903.1:n.55-46G>T
XM_011528941.2:c.55-46G>T	XP_011527243.1:n.55-46G>T
XM_017027986.1:c.55-46G>T	XP_016883475.1:n.55-46G>T
NM_020884.5:c.55-46G>T	NP_065935.3:n.55-46G>T
NM_020884.7:c.-72-46G>T MANE Select	NP_065935.4:n.-72-46G>T