Canonical Allele Identifier: CA408692325

Gene: MYH7B

Linked Data

• MyVariant Identifiers: chr20:g.33565764C>G (hg19) ; chr20:g.34977961C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34977961C>G , CM000682.2:g.34977961C>G	GRCh38
NC_000020.10:g.33565764C>G , CM000682.1:g.33565764C>G	GRCh37
NC_000020.9:g.33029425C>G	NCBI36
NG_016984.2:g.27061C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262873.13:c.-45C>G MANE Select	ENSP00000262873.8:n.-45C>G
ENST00000262873.12:c.-45C>G	ENSP00000262873.8:n.-45C>G
ENST00000618182.6:c.79C>G	ENSP00000483640.3:p.Leu27Val
ENST00000673749.1:n.490C>G
ENST00000262873.11:c.82C>G	ENSP00000262873.7:p.Leu28Val
ENST00000470929.5:n.42C>G
ENST00000618182.4:c.79C>G	ENSP00000483640.1:p.Leu27Val
NM_020884.4:c.82C>G	NP_065935.3:p.Leu28Val
XM_006723840.2:c.82C>G	XP_006723903.1:p.Leu28Val
XM_011528941.1:c.82C>G	XP_011527243.1:p.Leu28Val
XM_011528942.1:c.82C>G	XP_011527244.1:p.Leu28Val
XM_011528943.1:c.82C>G	XP_011527245.1:p.Leu28Val
XM_011528944.1:c.82C>G	XP_011527246.1:p.Leu28Val
XM_011528945.1:c.-428C>G	XP_011527247.1:n.-428C>G
XM_011528950.1:c.82C>G	XP_011527252.1:p.Leu28Val
XM_006723840.3:c.82C>G	XP_006723903.1:p.Leu28Val
XM_011528941.2:c.82C>G	XP_011527243.1:p.Leu28Val
XM_017027986.1:c.82C>G	XP_016883475.1:p.Leu28Val
NM_020884.5:c.82C>G	NP_065935.3:p.Leu28Val
NM_020884.7:c.-45C>G MANE Select	NP_065935.4:n.-45C>G