Canonical Allele Identifier: CA2082579220

Linked Data

dbSNP Id: rs1366756863

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.31872662G>T , CM000675.2:g.31872662G>T GRCh38
NC_000013.10:g.32446799G>T , CM000675.1:g.32446799G>T GRCh37
NC_000013.9:g.31344799G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645780.1:c.-254+25723G>T (FRY) ENSP00000494080.1:n.-254+25723G>T
ENST00000428783.1:n.99+25723G>T (EEF1DP3)
NR_027062.1:n.157+25723G>T (EEF1DP3)