Canonical Allele Identifier: CA2123455090
Community Standard Title: NM_000257.4(MYH7):c.211G= (p.Val71=)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433218C= , CM000676.2:g.23433218C= GRCh38
NC_000014.8:g.23902427C= , CM000676.1:g.23902427C= GRCh37
NC_000014.7:g.22972267C= NCBI36
NG_007884.1:g.7444G= , LRG_384:g.7444G=

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.211G= MANE Select NP_000248.2:p.Val71=
ENST00000355349.4:c.211G= MANE Select ENSP00000347507.3:p.Val71=
NM_000257.3:c.211G= NP_000248.2:p.Val71=
ENST00000355349.3:c.211G= ENSP00000347507.3:p.Val71=
XM_017021340.1:c.211G= XP_016876829.1:p.Val71=
XR_245686.3:n.317G=