Canonical Allele Identifier: CA2123451469
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431436A= , CM000676.2:g.23431436A= GRCh38
NC_000014.8:g.23900645A= , CM000676.1:g.23900645A= GRCh37
NC_000014.7:g.22970485A= NCBI36
NG_007884.1:g.9226T= , LRG_384:g.9226T=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.778T= MANE Select ENSP00000347507.3:p.Ser260=
ENST00000355349.3:c.778T= ENSP00000347507.3:p.Ser260=
NM_000257.3:c.778T= NP_000248.2:p.Ser260=
XR_245686.3:n.884T=
XM_017021340.1:c.778T= XP_016876829.1:p.Ser260=
NM_000257.4:c.778T= MANE Select NP_000248.2:p.Ser260=