Canonical Allele Identifier: CA4582275
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs760494561
ExAC: 7:152345710 C / CTAT
gnomAD v2: 7-152345710-C-CTAT
gnomAD v3: 7-152648625-C-CTAT
gnomAD v4: 7-152648625-C-CTAT
MyVariant Identifiers: chr7:g.152345710_152345711insTAT (hg19) chr7:g.152648625_152648626insTAT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648627_152648629dup , CM000669.2:g.152648627_152648629dup GRCh38
NC_000007.13:g.152345712_152345714dup , CM000669.1:g.152345712_152345714dup GRCh37
NC_000007.12:g.151976645_151976647dup NCBI36
NG_027988.1:g.32538_32540dup
NG_027988.2:g.32538_32540dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*14_*16dup ENSP00000513758.1:n.*14_*16dup
ENST00000359321.2:c.*14_*16dup MANE Select ENSP00000352271.1:n.*14_*16dup
ENST00000359321.1:c.*14_*16dup ENSP00000352271.1:n.*14_*16dup
ENST00000495707.1:n.879_881dup
NM_005431.1:c.*14_*16dup NP_005422.1:n.*14_*16dup
NM_005431.2:c.*14_*16dup MANE Select NP_005422.1:n.*14_*16dup
Search 100 bp 5'
Search 100 bp 3'