Canonical Allele Identifier: CA389053511
Community Standard Title: NM_000257.4(MYH7):c.209C>T (p.Thr70Ile)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433220G>A , CM000676.2:g.23433220G>A GRCh38
NC_000014.8:g.23902429G>A , CM000676.1:g.23902429G>A GRCh37
NC_000014.7:g.22972269G>A NCBI36
NG_007884.1:g.7442C>T , LRG_384:g.7442C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.209C>T MANE Select NP_000248.2:p.Thr70Ile
ENST00000355349.4:c.209C>T MANE Select ENSP00000347507.3:p.Thr70Ile
NM_000257.3:c.209C>T NP_000248.2:p.Thr70Ile
ENST00000355349.3:c.209C>T ENSP00000347507.3:p.Thr70Ile
XM_017021340.1:c.209C>T XP_016876829.1:p.Thr70Ile
XR_245686.3:n.315C>T