Canonical Allele Identifier: CA578933749

Gene: XRCC2

Linked Data

• dbSNP Id: rs761103083
• gnomAD v2: 7-152357743-T-G
• gnomAD v3: 7-152660658-T-G
• gnomAD v4: 7-152660658-T-G
• MyVariant Identifiers: chr7:g.152357743T>G (hg19) ; chr7:g.152660658T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152660658T>G , CM000669.2:g.152660658T>G	GRCh38
NC_000007.13:g.152357743T>G , CM000669.1:g.152357743T>G	GRCh37
NC_000007.12:g.151988676T>G	NCBI36
NG_027988.1:g.20508A>C
NG_027988.2:g.20508A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698506.1:c.-47-11295A>C	ENSP00000513758.1:n.-47-11295A>C
ENST00000698507.1:n.232A>C
ENST00000359321.2:c.121+43A>C MANE Select	ENSP00000352271.1:n.121+43A>C
ENST00000359321.1:c.121+43A>C	ENSP00000352271.1:n.121+43A>C
ENST00000495707.1:n.143+43A>C
NM_005431.1:c.121+43A>C	NP_005422.1:n.121+43A>C
NM_005431.2:c.121+43A>C MANE Select	NP_005422.1:n.121+43A>C