Canonical Allele Identifier: CA2685735647
Gene: XRCC2 HGNC NCBI

Linked Data

gnomAD v4: 7-152648510-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648510C>A , CM000669.2:g.152648510C>A GRCh38
NC_000007.13:g.152345595C>A , CM000669.1:g.152345595C>A GRCh37
NC_000007.12:g.151976528C>A NCBI36
NG_027988.1:g.32656G>T
NG_027988.2:g.32656G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*132G>T ENSP00000513758.1:n.*132G>T
ENST00000359321.2:c.*132G>T MANE Select ENSP00000352271.1:n.*132G>T
ENST00000359321.1:c.*132G>T ENSP00000352271.1:n.*132G>T
ENST00000495707.1:n.997G>T
NM_005431.1:c.*132G>T NP_005422.1:n.*132G>T
NM_005431.2:c.*132G>T MANE Select NP_005422.1:n.*132G>T
Search 100 bp 5'
Search 100 bp 3'