Canonical Allele Identifier: CA4582305
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418548
ClinVar RCV Id: RCV000478407 RCV001026307
dbSNP Id: rs749779141
ExAC: 7:152345836 T / C
gnomAD v2: 7-152345836-T-C
gnomAD v3: 7-152648751-T-C
gnomAD v4: 7-152648751-T-C
MyVariant Identifiers: chr7:g.152345836T>C (hg19) chr7:g.152648751T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648751T>C , CM000669.2:g.152648751T>C GRCh38
NC_000007.13:g.152345836T>C , CM000669.1:g.152345836T>C GRCh37
NC_000007.12:g.151976769T>C NCBI36
NG_027988.1:g.32415A>G
NG_027988.2:g.32415A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.566A>G ENSP00000513758.1:p.Asp189Gly
ENST00000359321.2:c.734A>G MANE Select ENSP00000352271.1:p.Asp245Gly
ENST00000359321.1:c.734A>G ENSP00000352271.1:p.Asp245Gly
ENST00000495707.1:n.756A>G
NM_005431.1:c.734A>G NP_005422.1:p.Asp245Gly
NM_005431.2:c.734A>G MANE Select NP_005422.1:p.Asp245Gly
Search 100 bp 5'
Search 100 bp 3'