Canonical Allele Identifier: CA2582752932

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12800391C>A , CM000681.2:g.12800391C>A GRCh38
NC_000019.9:g.12911205C>A , CM000681.1:g.12911205C>A GRCh37
NC_000019.8:g.12772205C>A NCBI36
NG_029901.1:g.6490G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000301522.3:c.258-92G>T (PRDX2) MANE Select ENSP00000301522.2:n.258-92G>T
ENST00000301522.2:c.258-92G>T (PRDX2) ENSP00000301522.2:n.258-92G>T
ENST00000334482.9:c.258-92G>T (PRDX2) ENSP00000334063.5:n.258-92G>T
ENST00000466174.5:n.841G>T (PRDX2)
ENST00000477555.1:n.316-92G>T (PRDX2)
ENST00000478908.1:n.71G>T (PRDX2)
ENST00000589765.1:n.41+24787G>T (HOOK2)
NM_005809.5:c.258-92G>T (PRDX2) NP_005800.3:n.258-92G>T
NM_005809.6:c.258-92G>T (PRDX2) MANE Select NP_005800.3:n.258-92G>T