Canonical Allele Identifier: CA954670253

Linked Data

dbSNP Id: rs1868415788

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.31872690T>A , CM000675.2:g.31872690T>A GRCh38
NC_000013.10:g.32446827T>A , CM000675.1:g.32446827T>A GRCh37
NC_000013.9:g.31344827T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645780.1:c.-254+25751T>A (FRY) ENSP00000494080.1:n.-254+25751T>A
ENST00000428783.1:n.99+25751T>A (EEF1DP3)
NR_027062.1:n.157+25751T>A (EEF1DP3)