Canonical Allele Identifier: CA370199577
Gene: XRCC2 HGNC NCBI

Linked Data

gnomAD v4: 7-152676045-G-C
MyVariant Identifiers: chr7:g.152373130G>C (hg19) chr7:g.152676045G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676045G>C , CM000669.2:g.152676045G>C GRCh38
NC_000007.13:g.152373130G>C , CM000669.1:g.152373130G>C GRCh37
NC_000007.12:g.152004063G>C NCBI36
NG_027988.1:g.5121C>G
NG_027988.2:g.5121C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-52C>G ENSP00000513758.1:n.-52C>G
ENST00000698507.1:n.103C>G
ENST00000359321.2:c.35C>G MANE Select ENSP00000352271.1:p.Thr12Ser
ENST00000359321.1:c.35C>G ENSP00000352271.1:p.Thr12Ser
NM_005431.1:c.35C>G NP_005422.1:p.Thr12Ser
NM_005431.2:c.35C>G MANE Select NP_005422.1:p.Thr12Ser
Search 100 bp 5'
Search 100 bp 3'