Canonical Allele Identifier: CA313462459

Gene: MYH7B

Linked Data

• dbSNP Id: rs11906160
• MyVariant Identifiers: chr20:g.33565755G>T (hg19) ; chr20:g.34977952G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34977952G>T , CM000682.2:g.34977952G>T	GRCh38
NC_000020.10:g.33565755G>T , CM000682.1:g.33565755G>T	GRCh37
NC_000020.9:g.33029416G>T	NCBI36
NG_016984.2:g.27052G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262873.13:c.-54G>T MANE Select	ENSP00000262873.8:n.-54G>T
ENST00000262873.12:c.-54G>T	ENSP00000262873.8:n.-54G>T
ENST00000618182.6:c.70G>T	ENSP00000483640.3:p.Ala24Ser
ENST00000673749.1:n.481G>T
ENST00000262873.11:c.73G>T	ENSP00000262873.7:p.Ala25Ser
ENST00000470929.5:n.33G>T
ENST00000618182.4:c.70G>T	ENSP00000483640.1:p.Ala24Ser
NM_020884.4:c.73G>T	NP_065935.3:p.Ala25Ser
XM_006723840.2:c.73G>T	XP_006723903.1:p.Ala25Ser
XM_011528941.1:c.73G>T	XP_011527243.1:p.Ala25Ser
XM_011528942.1:c.73G>T	XP_011527244.1:p.Ala25Ser
XM_011528943.1:c.73G>T	XP_011527245.1:p.Ala25Ser
XM_011528944.1:c.73G>T	XP_011527246.1:p.Ala25Ser
XM_011528945.1:c.-437G>T	XP_011527247.1:n.-437G>T
XM_011528950.1:c.73G>T	XP_011527252.1:p.Ala25Ser
XM_006723840.3:c.73G>T	XP_006723903.1:p.Ala25Ser
XM_011528941.2:c.73G>T	XP_011527243.1:p.Ala25Ser
XM_017027986.1:c.73G>T	XP_016883475.1:p.Ala25Ser
NM_020884.5:c.73G>T	NP_065935.3:p.Ala25Ser
NM_020884.7:c.-54G>T MANE Select	NP_065935.4:n.-54G>T