Canonical Allele Identifier: CA2082579236

Linked Data

dbSNP Id: rs1868415716

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.31872672A>C , CM000675.2:g.31872672A>C GRCh38
NC_000013.10:g.32446809A>C , CM000675.1:g.32446809A>C GRCh37
NC_000013.9:g.31344809A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645780.1:c.-254+25733A>C (FRY) ENSP00000494080.1:n.-254+25733A>C
ENST00000428783.1:n.99+25733A>C (EEF1DP3)
NR_027062.1:n.157+25733A>C (EEF1DP3)