Canonical Allele Identifier: CA2685735682
Gene: XRCC2 HGNC NCBI

Linked Data

gnomAD v4: 7-152648545-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648545C>A , CM000669.2:g.152648545C>A GRCh38
NC_000007.13:g.152345630C>A , CM000669.1:g.152345630C>A GRCh37
NC_000007.12:g.151976563C>A NCBI36
NG_027988.1:g.32621G>T
NG_027988.2:g.32621G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*97G>T ENSP00000513758.1:n.*97G>T
ENST00000359321.2:c.*97G>T MANE Select ENSP00000352271.1:n.*97G>T
ENST00000359321.1:c.*97G>T ENSP00000352271.1:n.*97G>T
ENST00000495707.1:n.962G>T
NM_005431.1:c.*97G>T NP_005422.1:n.*97G>T
NM_005431.2:c.*97G>T MANE Select NP_005422.1:n.*97G>T
Search 100 bp 5'
Search 100 bp 3'