Canonical Allele Identifier: CA954670259

Linked Data

dbSNP Id: rs1868420058

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.31872803T>A , CM000675.2:g.31872803T>A GRCh38
NC_000013.10:g.32446940T>A , CM000675.1:g.32446940T>A GRCh37
NC_000013.9:g.31344940T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645780.1:c.-254+25864T>A (FRY) ENSP00000494080.1:n.-254+25864T>A
ENST00000428783.1:n.99+25864T>A (EEF1DP3)
NR_027062.1:n.157+25864T>A (EEF1DP3)