Canonical Allele Identifier: CA2123452904
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431864T= , CM000676.2:g.23431864T= GRCh38
NC_000014.8:g.23901073T= , CM000676.1:g.23901073T= GRCh37
NC_000014.7:g.22970913T= NCBI36
NG_007884.1:g.8798A= , LRG_384:g.8798A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.536A= MANE Select ENSP00000347507.3:p.Glu179=
ENST00000355349.3:c.536A= ENSP00000347507.3:p.Glu179=
NM_000257.3:c.536A= NP_000248.2:p.Glu179=
XR_245686.3:n.642A=
XM_017021340.1:c.536A= XP_016876829.1:p.Glu179=
NM_000257.4:c.536A= MANE Select NP_000248.2:p.Glu179=