Canonical Allele Identifier: CA16605203
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 388556
ClinVar RCV Id: RCV000435944
dbSNP Id: rs1057523148
MyVariant Identifiers: chr7:g.152373193T>C (hg19) chr7:g.152676108T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676108T>C , CM000669.2:g.152676108T>C GRCh38
NC_000007.13:g.152373193T>C , CM000669.1:g.152373193T>C GRCh37
NC_000007.12:g.152004126T>C NCBI36
NG_027988.1:g.5058A>G
NG_027988.2:g.5058A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-115A>G ENSP00000513758.1:n.-115A>G
ENST00000698507.1:n.40A>G
ENST00000359321.2:c.-29A>G MANE Select ENSP00000352271.1:n.-29A>G
ENST00000359321.1:c.-29A>G ENSP00000352271.1:n.-29A>G
NM_005431.1:c.-29A>G NP_005422.1:n.-29A>G
NM_005431.2:c.-29A>G MANE Select NP_005422.1:n.-29A>G
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