Canonical Allele Identifier: CA2123454814
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424148T= , CM000676.2:g.23424148T= GRCh38
NC_000014.8:g.23893357T= , CM000676.1:g.23893357T= GRCh37
NC_000014.7:g.22963197T= NCBI36
NG_007884.1:g.16514A= , LRG_384:g.16514A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2681A= MANE Select ENSP00000347507.3:p.Glu894=
ENST00000355349.3:c.2681A= ENSP00000347507.3:p.Glu894=
NM_000257.3:c.2681A= NP_000248.2:p.Glu894=
XR_245686.3:n.2787A=
XM_017021340.1:c.2681A= XP_016876829.1:p.Glu894=
NM_000257.4:c.2681A= MANE Select NP_000248.2:p.Glu894=