Canonical Allele Identifier: CA012904
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 164316
dbSNP Id: rs727503253

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424119G>A , CM000676.2:g.23424119G>A GRCh38
NC_000014.8:g.23893328G>A , CM000676.1:g.23893328G>A GRCh37
NC_000014.7:g.22963168G>A NCBI36
NG_007884.1:g.16543C>T , LRG_384:g.16543C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2710C>T MANE Select ENSP00000347507.3:p.Arg904Cys
ENST00000355349.3:c.2710C>T ENSP00000347507.3:p.Arg904Cys
NM_000257.3:c.2710C>T NP_000248.2:p.Arg904Cys
XR_245686.3:n.2816C>T
XM_017021340.1:c.2710C>T XP_016876829.1:p.Arg904Cys
NM_000257.4:c.2710C>T MANE Select NP_000248.2:p.Arg904Cys