Canonical Allele Identifier: CA458805209
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1446744510
MyVariant Identifiers: chr7:g.152373129G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676044G>C , CM000669.2:g.152676044G>C GRCh38
NC_000007.13:g.152373129G>C , CM000669.1:g.152373129G>C GRCh37
NC_000007.12:g.152004062G>C NCBI36
NG_027988.1:g.5122C>G
NG_027988.2:g.5122C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-51C>G ENSP00000513758.1:n.-51C>G
ENST00000698507.1:n.104C>G
ENST00000359321.2:c.36C>G MANE Select ENSP00000352271.1:p.Thr12=
ENST00000359321.1:c.36C>G ENSP00000352271.1:p.Thr12=
NM_005431.1:c.36C>G NP_005422.1:p.Thr12=
NM_005431.2:c.36C>G MANE Select NP_005422.1:p.Thr12=
Search 100 bp 5'
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