Canonical Allele Identifier: CA389047986
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424828C>T , CM000676.2:g.23424828C>T GRCh38
NC_000014.8:g.23894037C>T , CM000676.1:g.23894037C>T GRCh37
NC_000014.7:g.22963877C>T NCBI36
NG_007884.1:g.15834G>A , LRG_384:g.15834G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2620G>A MANE Select ENSP00000347507.3:p.Glu874Lys
ENST00000355349.3:c.2620G>A ENSP00000347507.3:p.Glu874Lys
NM_000257.3:c.2620G>A NP_000248.2:p.Glu874Lys
XR_245686.3:n.2726G>A
XM_017021340.1:c.2620G>A XP_016876829.1:p.Glu874Lys
NM_000257.4:c.2620G>A MANE Select NP_000248.2:p.Glu874Lys