Canonical Allele Identifier: CA016701
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 14126
dbSNP Id: rs267606910

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431589C>T , CM000676.2:g.23431589C>T GRCh38
NC_000014.8:g.23900798C>T , CM000676.1:g.23900798C>T GRCh37
NC_000014.7:g.22970638C>T NCBI36
NG_007884.1:g.9073G>A , LRG_384:g.9073G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.728G>A MANE Select ENSP00000347507.3:p.Arg243His
ENST00000355349.3:c.728G>A ENSP00000347507.3:p.Arg243His
NM_000257.3:c.728G>A NP_000248.2:p.Arg243His
XR_245686.3:n.834G>A
XM_017021340.1:c.728G>A XP_016876829.1:p.Arg243His
NM_000257.4:c.728G>A MANE Select NP_000248.2:p.Arg243His