Canonical Allele Identifier: CA4582317
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs756194404
ExAC: 7:152345935 G / T
gnomAD v2: 7-152345935-G-T
gnomAD v3: 7-152648850-G-T
gnomAD v4: 7-152648850-G-T
MyVariant Identifiers: chr7:g.152345935G>T (hg19) chr7:g.152648850G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648850G>T , CM000669.2:g.152648850G>T GRCh38
NC_000007.13:g.152345935G>T , CM000669.1:g.152345935G>T GRCh37
NC_000007.12:g.151976868G>T NCBI36
NG_027988.1:g.32316C>A
NG_027988.2:g.32316C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.467C>A ENSP00000513758.1:p.Ala156Asp
ENST00000359321.2:c.635C>A MANE Select ENSP00000352271.1:p.Ala212Asp
ENST00000359321.1:c.635C>A ENSP00000352271.1:p.Ala212Asp
ENST00000495707.1:n.657C>A
NM_005431.1:c.635C>A NP_005422.1:p.Ala212Asp
NM_005431.2:c.635C>A MANE Select NP_005422.1:p.Ala212Asp
Search 100 bp 5'
Search 100 bp 3'