Canonical Allele Identifier: CA2123451135
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431323A= , CM000676.2:g.23431323A= GRCh38
NC_000014.8:g.23900532A= , CM000676.1:g.23900532A= GRCh37
NC_000014.7:g.22970372A= NCBI36
NG_007884.1:g.9339T= , LRG_384:g.9339T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.796+95T= MANE Select ENSP00000347507.3:n.796+95T=
ENST00000355349.3:c.796+95T= ENSP00000347507.3:n.796+95T=
NM_000257.3:c.796+95T= NP_000248.2:n.796+95T=
XR_245686.3:n.902+95T=
XM_017021340.1:c.796+95T= XP_016876829.1:n.796+95T=
NM_000257.4:c.796+95T= MANE Select NP_000248.2:n.796+95T=