Canonical Allele Identifier: CA2123452190
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431638G= , CM000676.2:g.23431638G= GRCh38
NC_000014.8:g.23900847G= , CM000676.1:g.23900847G= GRCh37
NC_000014.7:g.22970687G= NCBI36
NG_007884.1:g.9024C= , LRG_384:g.9024C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.679C= MANE Select ENSP00000347507.3:p.Leu227=
ENST00000355349.3:c.679C= ENSP00000347507.3:p.Leu227=
NM_000257.3:c.679C= NP_000248.2:p.Leu227=
XR_245686.3:n.785C=
XM_017021340.1:c.679C= XP_016876829.1:p.Leu227=
NM_000257.4:c.679C= MANE Select NP_000248.2:p.Leu227=