Canonical Allele Identifier: CA2685736271
Gene: XRCC2 HGNC NCBI

Linked Data

gnomAD v4: 7-152660573-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660573C>A , CM000669.2:g.152660573C>A GRCh38
NC_000007.13:g.152357658C>A , CM000669.1:g.152357658C>A GRCh37
NC_000007.12:g.151988591C>A NCBI36
NG_027988.1:g.20593G>T
NG_027988.2:g.20593G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-47-11210G>T ENSP00000513758.1:n.-47-11210G>T
ENST00000698507.1:n.317G>T
ENST00000359321.2:c.121+128G>T MANE Select ENSP00000352271.1:n.121+128G>T
ENST00000359321.1:c.121+128G>T ENSP00000352271.1:n.121+128G>T
ENST00000495707.1:n.143+128G>T
NM_005431.1:c.121+128G>T NP_005422.1:n.121+128G>T
NM_005431.2:c.121+128G>T MANE Select NP_005422.1:n.121+128G>T
Search 100 bp 5'
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