Canonical Allele Identifier: CA631839695

Linked Data

dbSNP Id: rs1224324320

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12800393G>C , CM000681.2:g.12800393G>C GRCh38
NC_000019.9:g.12911207G>C , CM000681.1:g.12911207G>C GRCh37
NC_000019.8:g.12772207G>C NCBI36
NG_029901.1:g.6488C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000301522.3:c.258-94C>G (PRDX2) MANE Select ENSP00000301522.2:n.258-94C>G
ENST00000301522.2:c.258-94C>G (PRDX2) ENSP00000301522.2:n.258-94C>G
ENST00000334482.9:c.258-94C>G (PRDX2) ENSP00000334063.5:n.258-94C>G
ENST00000466174.5:n.839C>G (PRDX2)
ENST00000477555.1:n.316-94C>G (PRDX2)
ENST00000478908.1:n.69C>G (PRDX2)
ENST00000589765.1:n.41+24785C>G (HOOK2)
NM_005809.5:c.258-94C>G (PRDX2) NP_005800.3:n.258-94C>G
NM_005809.6:c.258-94C>G (PRDX2) MANE Select NP_005800.3:n.258-94C>G