Canonical Allele Identifier: CA2123456390
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433890C= , CM000676.2:g.23433890C= GRCh38
NC_000014.8:g.23903099C= , CM000676.1:g.23903099C= GRCh37
NC_000014.7:g.22972939C= NCBI36
NG_007884.1:g.6772G= , LRG_384:g.6772G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.-8-150G= MANE Select ENSP00000347507.3:n.-8-150G=
ENST00000355349.3:c.-8-150G= ENSP00000347507.3:n.-8-150G=
NM_000257.3:c.-8-150G= NP_000248.2:n.-8-150G=
XR_245686.3:n.99-150G=
XM_017021340.1:c.-8-150G= XP_016876829.1:n.-8-150G=
NM_000257.4:c.-8-150G= MANE Select NP_000248.2:n.-8-150G=