Canonical Allele Identifier: CA2123450909
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431160G= , CM000676.2:g.23431160G= GRCh38
NC_000014.8:g.23900369G= , CM000676.1:g.23900369G= GRCh37
NC_000014.7:g.22970209G= NCBI36
NG_007884.1:g.9502C= , LRG_384:g.9502C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.797-161C= MANE Select ENSP00000347507.3:n.797-161C=
ENST00000355349.3:c.797-161C= ENSP00000347507.3:n.797-161C=
NM_000257.3:c.797-161C= NP_000248.2:n.797-161C=
XR_245686.3:n.903-161C=
XM_017021340.1:c.797-161C= XP_016876829.1:n.797-161C=
NM_000257.4:c.797-161C= MANE Select NP_000248.2:n.797-161C=