Canonical Allele Identifier: CA2123450988
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431206A= , CM000676.2:g.23431206A= GRCh38
NC_000014.8:g.23900415A= , CM000676.1:g.23900415A= GRCh37
NC_000014.7:g.22970255A= NCBI36
NG_007884.1:g.9456T= , LRG_384:g.9456T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.797-207T= MANE Select ENSP00000347507.3:n.797-207T=
ENST00000355349.3:c.797-207T= ENSP00000347507.3:n.797-207T=
NM_000257.3:c.797-207T= NP_000248.2:n.797-207T=
XR_245686.3:n.903-207T=
XM_017021340.1:c.797-207T= XP_016876829.1:n.797-207T=
NM_000257.4:c.797-207T= MANE Select NP_000248.2:n.797-207T=