Canonical Allele Identifier: CA3209386425
Community Standard Title: NM_000257.4(MYH7):c.202A= (p.Thr68=)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433227T= , CM000676.2:g.23433227T= GRCh38
NC_000014.8:g.23902436T= , CM000676.1:g.23902436T= GRCh37
NC_000014.7:g.22972276T= NCBI36
NG_007884.1:g.7435A= , LRG_384:g.7435A=

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.202A= MANE Select NP_000248.2:p.Thr68=
ENST00000355349.4:c.202A= MANE Select ENSP00000347507.3:p.Thr68=
NM_000257.3:c.202A= NP_000248.2:p.Thr68=
ENST00000355349.3:c.202A= ENSP00000347507.3:p.Thr68=
XM_017021340.1:c.202A= XP_016876829.1:p.Thr68=
XR_245686.3:n.308A=