Canonical Allele Identifier: CA2082579456

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.31872865G= , CM000675.2:g.31872865G= GRCh38
NC_000013.10:g.32447002G= , CM000675.1:g.32447002G= GRCh37
NC_000013.9:g.31345002G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645780.1:c.-254+25926G= (FRY) ENSP00000494080.1:n.-254+25926G=
ENST00000428783.1:n.99+25926G= (EEF1DP3)
NR_027062.1:n.157+25926G= (EEF1DP3)