Canonical Allele Identifier: CA2582753076

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12800502C>A , CM000681.2:g.12800502C>A GRCh38
NC_000019.9:g.12911316C>A , CM000681.1:g.12911316C>A GRCh37
NC_000019.8:g.12772316C>A NCBI36
NG_029901.1:g.6379G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301522.3:c.258-203G>T (PRDX2) MANE Select ENSP00000301522.2:n.258-203G>T
ENST00000301522.2:c.258-203G>T (PRDX2) ENSP00000301522.2:n.258-203G>T
ENST00000334482.9:c.258-203G>T (PRDX2) ENSP00000334063.5:n.258-203G>T
ENST00000466174.5:n.730G>T (PRDX2)
ENST00000477555.1:n.316-203G>T (PRDX2)
ENST00000589765.1:n.41+24676G>T (HOOK2)
NM_005809.5:c.258-203G>T (PRDX2) NP_005800.3:n.258-203G>T
NM_005809.6:c.258-203G>T (PRDX2) MANE Select NP_005800.3:n.258-203G>T