Canonical Allele Identifier: CA4582332
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs754995556
ExAC: 7:152346040 G / C
gnomAD v2: 7-152346040-G-C
gnomAD v4: 7-152648955-G-C
MyVariant Identifiers: chr7:g.152346040G>C (hg19) chr7:g.152648955G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648955G>C , CM000669.2:g.152648955G>C GRCh38
NC_000007.13:g.152346040G>C , CM000669.1:g.152346040G>C GRCh37
NC_000007.12:g.151976973G>C NCBI36
NG_027988.1:g.32211C>G
NG_027988.2:g.32211C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.362C>G ENSP00000513758.1:p.Ser121Cys
ENST00000359321.2:c.530C>G MANE Select ENSP00000352271.1:p.Ser177Cys
ENST00000359321.1:c.530C>G ENSP00000352271.1:p.Ser177Cys
ENST00000495707.1:n.552C>G
NM_005431.1:c.530C>G NP_005422.1:p.Ser177Cys
NM_005431.2:c.530C>G MANE Select NP_005422.1:p.Ser177Cys
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