Canonical Allele Identifier: CA012871
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181199
dbSNP Id: rs730880753

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424133G>T , CM000676.2:g.23424133G>T GRCh38
NC_000014.8:g.23893342G>T , CM000676.1:g.23893342G>T GRCh37
NC_000014.7:g.22963182G>T NCBI36
NG_007884.1:g.16529C>A , LRG_384:g.16529C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2696C>A MANE Select ENSP00000347507.3:p.Ala899Glu
ENST00000355349.3:c.2696C>A ENSP00000347507.3:p.Ala899Glu
NM_000257.3:c.2696C>A NP_000248.2:p.Ala899Glu
XR_245686.3:n.2802C>A
XM_017021340.1:c.2696C>A XP_016876829.1:p.Ala899Glu
NM_000257.4:c.2696C>A MANE Select NP_000248.2:p.Ala899Glu