Canonical Allele Identifier: CA835365516
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1424995744
gnomAD v3: 7-152675949-C-CA
gnomAD v4: 7-152675949-C-CA
MyVariant Identifiers: chr7:g.152373034_152373035insA (hg19) chr7:g.152675949_152675950insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152675951dup , CM000669.2:g.152675951dup GRCh38
NC_000007.13:g.152373036dup , CM000669.1:g.152373036dup GRCh37
NC_000007.12:g.152003969dup NCBI36
NG_027988.1:g.5216dup
NG_027988.2:g.5216dup

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-48+91dup ENSP00000513758.1:n.-48+91dup
ENST00000698507.1:n.107+91dup
ENST00000359321.2:c.39+91dup MANE Select ENSP00000352271.1:n.39+91dup
ENST00000359321.1:c.39+91dup ENSP00000352271.1:n.39+91dup
NM_005431.1:c.39+91dup NP_005422.1:n.39+91dup
NM_005431.2:c.39+91dup MANE Select NP_005422.1:n.39+91dup
Search 100 bp 5'
Search 100 bp 3'