Canonical Allele Identifier: CA1753219598
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs3218499
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152655054C>T , CM000669.2:g.152655054C>T GRCh38
NC_000007.13:g.152352139C>T , CM000669.1:g.152352139C>T GRCh37
NC_000007.12:g.151983072C>T NCBI36
NG_027988.1:g.26112G>A
NG_027988.2:g.26112G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-47-5691G>A ENSP00000513758.1:n.-47-5691G>A
ENST00000359321.2:c.121+5647G>A MANE Select ENSP00000352271.1:n.121+5647G>A
ENST00000359321.1:c.121+5647G>A ENSP00000352271.1:n.121+5647G>A
ENST00000495707.1:n.143+5647G>A
NM_005431.1:c.121+5647G>A NP_005422.1:n.121+5647G>A
NM_005431.2:c.121+5647G>A MANE Select NP_005422.1:n.121+5647G>A
Search 100 bp 5'
Search 100 bp 3'