Canonical Allele Identifier: CA408692319

Gene: MYH7B

Linked Data

• dbSNP Id: rs1162277246
• gnomAD v3: 20-34977959-A-C
• gnomAD v4: 20-34977959-A-C
• MyVariant Identifiers: chr20:g.33565762A>C (hg19) ; chr20:g.34977959A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34977959A>C , CM000682.2:g.34977959A>C	GRCh38
NC_000020.10:g.33565762A>C , CM000682.1:g.33565762A>C	GRCh37
NC_000020.9:g.33029423A>C	NCBI36
NG_016984.2:g.27059A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262873.13:c.-47A>C MANE Select	ENSP00000262873.8:n.-47A>C
ENST00000262873.12:c.-47A>C	ENSP00000262873.8:n.-47A>C
ENST00000618182.6:c.77A>C	ENSP00000483640.3:p.Asn26Thr
ENST00000673749.1:n.488A>C
ENST00000262873.11:c.80A>C	ENSP00000262873.7:p.Asn27Thr
ENST00000470929.5:n.40A>C
ENST00000618182.4:c.77A>C	ENSP00000483640.1:p.Asn26Thr
NM_020884.4:c.80A>C	NP_065935.3:p.Asn27Thr
XM_006723840.2:c.80A>C	XP_006723903.1:p.Asn27Thr
XM_011528941.1:c.80A>C	XP_011527243.1:p.Asn27Thr
XM_011528942.1:c.80A>C	XP_011527244.1:p.Asn27Thr
XM_011528943.1:c.80A>C	XP_011527245.1:p.Asn27Thr
XM_011528944.1:c.80A>C	XP_011527246.1:p.Asn27Thr
XM_011528945.1:c.-430A>C	XP_011527247.1:n.-430A>C
XM_011528950.1:c.80A>C	XP_011527252.1:p.Asn27Thr
XM_006723840.3:c.80A>C	XP_006723903.1:p.Asn27Thr
XM_011528941.2:c.80A>C	XP_011527243.1:p.Asn27Thr
XM_017027986.1:c.80A>C	XP_016883475.1:p.Asn27Thr
NM_020884.5:c.80A>C	NP_065935.3:p.Asn27Thr
NM_020884.7:c.-47A>C MANE Select	NP_065935.4:n.-47A>C