Canonical Allele Identifier: CA2685735676
Gene: XRCC2 HGNC NCBI

Linked Data

gnomAD v4: 7-152648541-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648541G>T , CM000669.2:g.152648541G>T GRCh38
NC_000007.13:g.152345626G>T , CM000669.1:g.152345626G>T GRCh37
NC_000007.12:g.151976559G>T NCBI36
NG_027988.1:g.32625C>A
NG_027988.2:g.32625C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*101C>A ENSP00000513758.1:n.*101C>A
ENST00000359321.2:c.*101C>A MANE Select ENSP00000352271.1:n.*101C>A
ENST00000359321.1:c.*101C>A ENSP00000352271.1:n.*101C>A
ENST00000495707.1:n.966C>A
NM_005431.1:c.*101C>A NP_005422.1:n.*101C>A
NM_005431.2:c.*101C>A MANE Select NP_005422.1:n.*101C>A
Search 100 bp 5'
Search 100 bp 3'