Canonical Allele Identifier: CA578935844
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs913908127
gnomAD v2: 7-152373090-T-G
gnomAD v4: 7-152676005-T-G
MyVariant Identifiers: chr7:g.152373090T>G (hg19) chr7:g.152676005T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676005T>G , CM000669.2:g.152676005T>G GRCh38
NC_000007.13:g.152373090T>G , CM000669.1:g.152373090T>G GRCh37
NC_000007.12:g.152004023T>G NCBI36
NG_027988.1:g.5161A>C
NG_027988.2:g.5161A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-48+36A>C ENSP00000513758.1:n.-48+36A>C
ENST00000698507.1:n.107+36A>C
ENST00000359321.2:c.39+36A>C MANE Select ENSP00000352271.1:n.39+36A>C
ENST00000359321.1:c.39+36A>C ENSP00000352271.1:n.39+36A>C
NM_005431.1:c.39+36A>C NP_005422.1:n.39+36A>C
NM_005431.2:c.39+36A>C MANE Select NP_005422.1:n.39+36A>C
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