Canonical Allele Identifier: CA2323577439

Linked Data

dbSNP Id: rs1599527999

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12800479A>G , CM000681.2:g.12800479A>G GRCh38
NC_000019.9:g.12911293A>G , CM000681.1:g.12911293A>G GRCh37
NC_000019.8:g.12772293A>G NCBI36
NG_029901.1:g.6402T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000301522.3:c.258-180T>C (PRDX2) MANE Select ENSP00000301522.2:n.258-180T>C
ENST00000301522.2:c.258-180T>C (PRDX2) ENSP00000301522.2:n.258-180T>C
ENST00000334482.9:c.258-180T>C (PRDX2) ENSP00000334063.5:n.258-180T>C
ENST00000466174.5:n.753T>C (PRDX2)
ENST00000477555.1:n.316-180T>C (PRDX2)
ENST00000589765.1:n.41+24699T>C (HOOK2)
NM_005809.5:c.258-180T>C (PRDX2) NP_005800.3:n.258-180T>C
NM_005809.6:c.258-180T>C (PRDX2) MANE Select NP_005800.3:n.258-180T>C