Canonical Allele Identifier: CA15947519

Linked Data

dbSNP Id: rs10427027

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12800471T>C , CM000681.2:g.12800471T>C GRCh38
NC_000019.9:g.12911285T>C , CM000681.1:g.12911285T>C GRCh37
NC_000019.8:g.12772285T>C NCBI36
NG_029901.1:g.6410A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000301522.3:c.258-172A>G (PRDX2) MANE Select ENSP00000301522.2:n.258-172A>G
ENST00000301522.2:c.258-172A>G (PRDX2) ENSP00000301522.2:n.258-172A>G
ENST00000334482.9:c.258-172A>G (PRDX2) ENSP00000334063.5:n.258-172A>G
ENST00000466174.5:n.761A>G (PRDX2)
ENST00000477555.1:n.316-172A>G (PRDX2)
ENST00000589765.1:n.41+24707A>G (HOOK2)
NM_005809.5:c.258-172A>G (PRDX2) NP_005800.3:n.258-172A>G
NM_005809.6:c.258-172A>G (PRDX2) MANE Select NP_005800.3:n.258-172A>G