Canonical Allele Identifier: CA2123455112
Community Standard Title: NM_000257.4(MYH7):c.209C= (p.Thr70=)
Gene: MYH7 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.209C= MANE Select NP_000248.2:p.Thr70=
ENST00000355349.4:c.209C= MANE Select ENSP00000347507.3:p.Thr70=
NM_000257.3:c.209C= NP_000248.2:p.Thr70=
ENST00000355349.3:c.209C= ENSP00000347507.3:p.Thr70=
XM_017021340.1:c.209C= XP_016876829.1:p.Thr70=
XR_245686.3:n.315C=