Canonical Allele Identifier: CA2123452348
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431682A= , CM000676.2:g.23431682A= GRCh38
NC_000014.8:g.23900891A= , CM000676.1:g.23900891A= GRCh37
NC_000014.7:g.22970731A= NCBI36
NG_007884.1:g.8980T= , LRG_384:g.8980T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.640-5T= MANE Select ENSP00000347507.3:n.640-5T=
ENST00000355349.3:c.640-5T= ENSP00000347507.3:n.640-5T=
NM_000257.3:c.640-5T= NP_000248.2:n.640-5T=
XR_245686.3:n.746-5T=
XM_017021340.1:c.640-5T= XP_016876829.1:n.640-5T=
NM_000257.4:c.640-5T= MANE Select NP_000248.2:n.640-5T=