Canonical Allele Identifier: CA2018007687
Community Standard Title: NC_000013.11:g.31873085A=

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.31873085A= , CM000675.2:g.31873085A= GRCh38
NC_000013.10:g.32447222A= , CM000675.1:g.32447222A= GRCh37
NC_000013.9:g.31345222A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027062.1:n.157+26146A= (EEF1DP3)
ENST00000428783.1:n.99+26146A= (EEF1DP3)
ENST00000645780.1:c.-254+26146A= (FRY) ENSP00000494080.1:n.-254+26146A=