Canonical Allele Identifier: CA2123448255
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23420794C= , CM000676.2:g.23420794C= GRCh38
NC_000014.8:g.23890003C= , CM000676.1:g.23890003C= GRCh37
NC_000014.7:g.22959843C= NCBI36
NG_007884.1:g.19868G= , LRG_384:g.19868G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3336+164G= MANE Select ENSP00000347507.3:n.3336+164G=
ENST00000355349.3:c.3336+164G= ENSP00000347507.3:n.3336+164G=
NM_000257.3:c.3336+164G= NP_000248.2:n.3336+164G=
XR_245686.3:n.3444+164G=
XM_017021340.1:c.3336+164G= XP_016876829.1:n.3336+164G=
NM_000257.4:c.3336+164G= MANE Select NP_000248.2:n.3336+164G=