Canonical Allele Identifier: CA408692310

Gene: MYH7B

Linked Data

• dbSNP Id: rs1363132814
• gnomAD v3: 20-34977955-T-G
• gnomAD v4: 20-34977955-T-G
• MyVariant Identifiers: chr20:g.33565758T>G (hg19) ; chr20:g.34977955T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34977955T>G , CM000682.2:g.34977955T>G	GRCh38
NC_000020.10:g.33565758T>G , CM000682.1:g.33565758T>G	GRCh37
NC_000020.9:g.33029419T>G	NCBI36
NG_016984.2:g.27055T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262873.13:c.-51T>G MANE Select	ENSP00000262873.8:n.-51T>G
ENST00000262873.12:c.-51T>G	ENSP00000262873.8:n.-51T>G
ENST00000618182.6:c.73T>G	ENSP00000483640.3:p.Leu25Val
ENST00000673749.1:n.484T>G
ENST00000262873.11:c.76T>G	ENSP00000262873.7:p.Leu26Val
ENST00000470929.5:n.36T>G
ENST00000618182.4:c.73T>G	ENSP00000483640.1:p.Leu25Val
NM_020884.4:c.76T>G	NP_065935.3:p.Leu26Val
XM_006723840.2:c.76T>G	XP_006723903.1:p.Leu26Val
XM_011528941.1:c.76T>G	XP_011527243.1:p.Leu26Val
XM_011528942.1:c.76T>G	XP_011527244.1:p.Leu26Val
XM_011528943.1:c.76T>G	XP_011527245.1:p.Leu26Val
XM_011528944.1:c.76T>G	XP_011527246.1:p.Leu26Val
XM_011528945.1:c.-434T>G	XP_011527247.1:n.-434T>G
XM_011528950.1:c.76T>G	XP_011527252.1:p.Leu26Val
XM_006723840.3:c.76T>G	XP_006723903.1:p.Leu26Val
XM_011528941.2:c.76T>G	XP_011527243.1:p.Leu26Val
XM_017027986.1:c.76T>G	XP_016883475.1:p.Leu26Val
NM_020884.5:c.76T>G	NP_065935.3:p.Leu26Val
NM_020884.7:c.-51T>G MANE Select	NP_065935.4:n.-51T>G