Canonical Allele Identifier: CA835376672
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1208245604
gnomAD v3: 7-152648404-T-A
gnomAD v4: 7-152648404-T-A
MyVariant Identifiers: chr7:g.152345489T>A (hg19) chr7:g.152648404T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648404T>A , CM000669.2:g.152648404T>A GRCh38
NC_000007.13:g.152345489T>A , CM000669.1:g.152345489T>A GRCh37
NC_000007.12:g.151976422T>A NCBI36
NG_027988.1:g.32762A>T
NG_027988.2:g.32762A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*238A>T ENSP00000513758.1:n.*238A>T
ENST00000359321.2:c.*238A>T MANE Select ENSP00000352271.1:n.*238A>T
ENST00000359321.1:c.*238A>T ENSP00000352271.1:n.*238A>T
ENST00000495707.1:n.1103A>T
NM_005431.1:c.*238A>T NP_005422.1:n.*238A>T
NM_005431.2:c.*238A>T MANE Select NP_005422.1:n.*238A>T
Search 100 bp 5'
Search 100 bp 3'