Canonical Allele Identifier: CA2082579120

Linked Data

dbSNP Id: rs1868414673

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.31872608C>T , CM000675.2:g.31872608C>T GRCh38
NC_000013.10:g.32446745C>T , CM000675.1:g.32446745C>T GRCh37
NC_000013.9:g.31344745C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645780.1:c.-254+25669C>T (FRY) ENSP00000494080.1:n.-254+25669C>T
ENST00000428783.1:n.99+25669C>T (EEF1DP3)
NR_027062.1:n.157+25669C>T (EEF1DP3)