Canonical Allele Identifier: CA2082579147

Linked Data

dbSNP Id: rs1868414911

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.31872620G>T , CM000675.2:g.31872620G>T GRCh38
NC_000013.10:g.32446757G>T , CM000675.1:g.32446757G>T GRCh37
NC_000013.9:g.31344757G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645780.1:c.-254+25681G>T (FRY) ENSP00000494080.1:n.-254+25681G>T
ENST00000428783.1:n.99+25681G>T (EEF1DP3)
NR_027062.1:n.157+25681G>T (EEF1DP3)