Canonical Allele Identifier: CA16568493

Linked Data

dbSNP Id: rs12151144

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12801582A>C , CM000681.2:g.12801582A>C GRCh38
NC_000019.9:g.12912396A>C , CM000681.1:g.12912396A>C GRCh37
NC_000019.8:g.12773396A>C NCBI36
NG_029901.1:g.5299T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000301522.3:c.-10+158T>G (PRDX2) MANE Select ENSP00000301522.2:n.-10+158T>G
ENST00000301522.2:c.-10+158T>G (PRDX2) ENSP00000301522.2:n.-10+158T>G
ENST00000334482.9:c.-10+158T>G (PRDX2) ENSP00000334063.5:n.-10+158T>G
ENST00000466174.5:n.50+158T>G (PRDX2)
ENST00000477555.1:n.49+158T>G (PRDX2)
ENST00000589765.1:n.41+23596T>G (HOOK2)
NM_005809.5:c.-10+158T>G (PRDX2) NP_005800.3:n.-10+158T>G
NM_005809.6:c.-10+158T>G (PRDX2) MANE Select NP_005800.3:n.-10+158T>G