Canonical Allele Identifier: CA247943102

Linked Data

dbSNP Id: rs1032188324

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.31872743T>G , CM000675.2:g.31872743T>G GRCh38
NC_000013.10:g.32446880T>G , CM000675.1:g.32446880T>G GRCh37
NC_000013.9:g.31344880T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645780.1:c.-254+25804T>G (FRY) ENSP00000494080.1:n.-254+25804T>G
ENST00000428783.1:n.99+25804T>G (EEF1DP3)
NR_027062.1:n.157+25804T>G (EEF1DP3)