Canonical Allele Identifier: CA408692313

Gene: MYH7B

Linked Data

• COSMIC: COSM6380736
• MyVariant Identifiers: chr20:g.33565759T>C (hg19) ; chr20:g.34977956T>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262873.13:c.-50T>C MANE Select	ENSP00000262873.8:n.-50T>C
ENST00000262873.12:c.-50T>C	ENSP00000262873.8:n.-50T>C
ENST00000618182.6:c.74T>C	ENSP00000483640.3:p.Leu25Ser
ENST00000673749.1:n.485T>C
ENST00000262873.11:c.77T>C	ENSP00000262873.7:p.Leu26Ser
ENST00000470929.5:n.37T>C
ENST00000618182.4:c.74T>C	ENSP00000483640.1:p.Leu25Ser
NM_020884.4:c.77T>C	NP_065935.3:p.Leu26Ser
XM_006723840.2:c.77T>C	XP_006723903.1:p.Leu26Ser
XM_011528941.1:c.77T>C	XP_011527243.1:p.Leu26Ser
XM_011528942.1:c.77T>C	XP_011527244.1:p.Leu26Ser
XM_011528943.1:c.77T>C	XP_011527245.1:p.Leu26Ser
XM_011528944.1:c.77T>C	XP_011527246.1:p.Leu26Ser
XM_011528945.1:c.-433T>C	XP_011527247.1:n.-433T>C
XM_011528950.1:c.77T>C	XP_011527252.1:p.Leu26Ser
XM_006723840.3:c.77T>C	XP_006723903.1:p.Leu26Ser
XM_011528941.2:c.77T>C	XP_011527243.1:p.Leu26Ser
XM_017027986.1:c.77T>C	XP_016883475.1:p.Leu26Ser
NM_020884.5:c.77T>C	NP_065935.3:p.Leu26Ser
NM_020884.7:c.-50T>C MANE Select	NP_065935.4:n.-50T>C