Canonical Allele Identifier: CA016828
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181326
dbSNP Id: rs730880855

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431425T>C , CM000676.2:g.23431425T>C GRCh38
NC_000014.8:g.23900634T>C , CM000676.1:g.23900634T>C GRCh37
NC_000014.7:g.22970474T>C NCBI36
NG_007884.1:g.9237A>G , LRG_384:g.9237A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.789A>G MANE Select ENSP00000347507.3:p.Ile263Met
ENST00000355349.3:c.789A>G ENSP00000347507.3:p.Ile263Met
NM_000257.3:c.789A>G NP_000248.2:p.Ile263Met
XR_245686.3:n.895A>G
XM_017021340.1:c.789A>G XP_016876829.1:p.Ile263Met
NM_000257.4:c.789A>G MANE Select NP_000248.2:p.Ile263Met