Canonical Allele Identifier: CA835376755
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1242923732
gnomAD v3: 7-152648444-C-T
gnomAD v4: 7-152648444-C-T
MyVariant Identifiers: chr7:g.152345529C>T (hg19) chr7:g.152648444C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648444C>T , CM000669.2:g.152648444C>T GRCh38
NC_000007.13:g.152345529C>T , CM000669.1:g.152345529C>T GRCh37
NC_000007.12:g.151976462C>T NCBI36
NG_027988.1:g.32722G>A
NG_027988.2:g.32722G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*198G>A ENSP00000513758.1:n.*198G>A
ENST00000359321.2:c.*198G>A MANE Select ENSP00000352271.1:n.*198G>A
ENST00000359321.1:c.*198G>A ENSP00000352271.1:n.*198G>A
ENST00000495707.1:n.1063G>A
NM_005431.1:c.*198G>A NP_005422.1:n.*198G>A
NM_005431.2:c.*198G>A MANE Select NP_005422.1:n.*198G>A
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