Canonical Allele Identifier: CA1108857353
Gene: XRCC2 HGNC NCBI

Linked Data

gnomAD v3: 7-152648405-T-G
gnomAD v4: 7-152648405-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648405T>G , CM000669.2:g.152648405T>G GRCh38
NC_000007.13:g.152345490T>G , CM000669.1:g.152345490T>G GRCh37
NC_000007.12:g.151976423T>G NCBI36
NG_027988.1:g.32761A>C
NG_027988.2:g.32761A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*237A>C ENSP00000513758.1:n.*237A>C
ENST00000359321.2:c.*237A>C MANE Select ENSP00000352271.1:n.*237A>C
ENST00000359321.1:c.*237A>C ENSP00000352271.1:n.*237A>C
ENST00000495707.1:n.1102A>C
NM_005431.1:c.*237A>C NP_005422.1:n.*237A>C
NM_005431.2:c.*237A>C MANE Select NP_005422.1:n.*237A>C
Search 100 bp 5'
Search 100 bp 3'