Canonical Allele Identifier: CA3209386320
Community Standard Title: NM_000257.4(MYH7):c.206T= (p.Val69=)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433223A= , CM000676.2:g.23433223A= GRCh38
NC_000014.8:g.23902432A= , CM000676.1:g.23902432A= GRCh37
NC_000014.7:g.22972272A= NCBI36
NG_007884.1:g.7439T= , LRG_384:g.7439T=

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.206T= MANE Select NP_000248.2:p.Val69=
ENST00000355349.4:c.206T= MANE Select ENSP00000347507.3:p.Val69=
NM_000257.3:c.206T= NP_000248.2:p.Val69=
ENST00000355349.3:c.206T= ENSP00000347507.3:p.Val69=
XM_017021340.1:c.206T= XP_016876829.1:p.Val69=
XR_245686.3:n.312T=