Canonical Allele Identifier: CA485626735
Community Standard Title: NM_000257.4(MYH7):c.303G>T (p.Val101=)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433126C>A , CM000676.2:g.23433126C>A GRCh38
NC_000014.8:g.23902335C>A , CM000676.1:g.23902335C>A GRCh37
NC_000014.7:g.22972175C>A NCBI36
NG_007884.1:g.7536G>T , LRG_384:g.7536G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.303G>T MANE Select NP_000248.2:p.Val101=
ENST00000355349.4:c.303G>T MANE Select ENSP00000347507.3:p.Val101=
NM_000257.3:c.303G>T NP_000248.2:p.Val101=
ENST00000355349.3:c.303G>T ENSP00000347507.3:p.Val101=
XM_017021340.1:c.303G>T XP_016876829.1:p.Val101=
XR_245686.3:n.409G>T