Canonical Allele Identifier: CA2123451776
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431490A= , CM000676.2:g.23431490A= GRCh38
NC_000014.8:g.23900699A= , CM000676.1:g.23900699A= GRCh37
NC_000014.7:g.22970539A= NCBI36
NG_007884.1:g.9172T= , LRG_384:g.9172T=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.733-9T= MANE Select ENSP00000347507.3:n.733-9T=
ENST00000355349.3:c.733-9T= ENSP00000347507.3:n.733-9T=
NM_000257.3:c.733-9T= NP_000248.2:n.733-9T=
XR_245686.3:n.839-9T=
XM_017021340.1:c.733-9T= XP_016876829.1:n.733-9T=
NM_000257.4:c.733-9T= MANE Select NP_000248.2:n.733-9T=