Canonical Allele Identifier: CA047607
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1107978
ClinVar RCV Id: RCV001433320
dbSNP Id: rs745823988

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431842G>A , CM000676.2:g.23431842G>A GRCh38
NC_000014.8:g.23901051G>A , CM000676.1:g.23901051G>A GRCh37
NC_000014.7:g.22970891G>A NCBI36
NG_007884.1:g.8820C>T , LRG_384:g.8820C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.558C>T MANE Select ENSP00000347507.3:p.Val186=
ENST00000355349.3:c.558C>T ENSP00000347507.3:p.Val186=
NM_000257.3:c.558C>T NP_000248.2:p.Val186=
XR_245686.3:n.664C>T
XM_017021340.1:c.558C>T XP_016876829.1:p.Val186=
NM_000257.4:c.558C>T MANE Select NP_000248.2:p.Val186=