Canonical Allele Identifier: CA2685736296
Gene: XRCC2 HGNC NCBI

Linked Data

gnomAD v4: 7-152660590-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660590C>G , CM000669.2:g.152660590C>G GRCh38
NC_000007.13:g.152357675C>G , CM000669.1:g.152357675C>G GRCh37
NC_000007.12:g.151988608C>G NCBI36
NG_027988.1:g.20576G>C
NG_027988.2:g.20576G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-47-11227G>C ENSP00000513758.1:n.-47-11227G>C
ENST00000698507.1:n.300G>C
ENST00000359321.2:c.121+111G>C MANE Select ENSP00000352271.1:n.121+111G>C
ENST00000359321.1:c.121+111G>C ENSP00000352271.1:n.121+111G>C
ENST00000495707.1:n.143+111G>C
NM_005431.1:c.121+111G>C NP_005422.1:n.121+111G>C
NM_005431.2:c.121+111G>C MANE Select NP_005422.1:n.121+111G>C
Search 100 bp 5'
Search 100 bp 3'