Canonical Allele Identifier: CA031227
Community Standard Title: NM_000257.4(MYH7):c.210C>T (p.Thr70=)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433219G>A , CM000676.2:g.23433219G>A GRCh38
NC_000014.8:g.23902428G>A , CM000676.1:g.23902428G>A GRCh37
NC_000014.7:g.22972268G>A NCBI36
NG_007884.1:g.7443C>T , LRG_384:g.7443C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.210C>T MANE Select NP_000248.2:p.Thr70=
ENST00000355349.4:c.210C>T MANE Select ENSP00000347507.3:p.Thr70=
NM_000257.3:c.210C>T NP_000248.2:p.Thr70=
ENST00000355349.3:c.210C>T ENSP00000347507.3:p.Thr70=
XM_017021340.1:c.210C>T XP_016876829.1:p.Thr70=
XR_245686.3:n.316C>T