Canonical Allele Identifier: CA408692331

Gene: MYH7B

Linked Data

• MyVariant Identifiers: chr20:g.33565767C>A (hg19) ; chr20:g.34977964C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34977964C>A , CM000682.2:g.34977964C>A	GRCh38
NC_000020.10:g.33565767C>A , CM000682.1:g.33565767C>A	GRCh37
NC_000020.9:g.33029428C>A	NCBI36
NG_016984.2:g.27064C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262873.13:c.-42C>A MANE Select	ENSP00000262873.8:n.-42C>A
ENST00000262873.12:c.-42C>A	ENSP00000262873.8:n.-42C>A
ENST00000618182.6:c.82C>A	ENSP00000483640.3:p.Gln28Lys
ENST00000673749.1:n.493C>A
ENST00000262873.11:c.85C>A	ENSP00000262873.7:p.Gln29Lys
ENST00000470929.5:n.45C>A
ENST00000618182.4:c.82C>A	ENSP00000483640.1:p.Gln28Lys
NM_020884.4:c.85C>A	NP_065935.3:p.Gln29Lys
XM_006723840.2:c.85C>A	XP_006723903.1:p.Gln29Lys
XM_011528941.1:c.85C>A	XP_011527243.1:p.Gln29Lys
XM_011528942.1:c.85C>A	XP_011527244.1:p.Gln29Lys
XM_011528943.1:c.85C>A	XP_011527245.1:p.Gln29Lys
XM_011528944.1:c.85C>A	XP_011527246.1:p.Gln29Lys
XM_011528945.1:c.-425C>A	XP_011527247.1:n.-425C>A
XM_011528950.1:c.85C>A	XP_011527252.1:p.Gln29Lys
XM_006723840.3:c.85C>A	XP_006723903.1:p.Gln29Lys
XM_011528941.2:c.85C>A	XP_011527243.1:p.Gln29Lys
XM_017027986.1:c.85C>A	XP_016883475.1:p.Gln29Lys
NM_020884.5:c.85C>A	NP_065935.3:p.Gln29Lys
NM_020884.7:c.-42C>A MANE Select	NP_065935.4:n.-42C>A