Canonical Allele Identifier: CA12551285

Gene: XRCC2

Linked Data

• dbSNP Id: rs3218499
• gnomAD v2: 7-152352139-C-G
• gnomAD v3: 7-152655054-C-G
• gnomAD v4: 7-152655054-C-G
• MyVariant Identifiers: chr7:g.152352139C>G (hg19) ; chr7:g.152655054C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152655054C>G , CM000669.2:g.152655054C>G	GRCh38
NC_000007.13:g.152352139C>G , CM000669.1:g.152352139C>G	GRCh37
NC_000007.12:g.151983072C>G	NCBI36
NG_027988.1:g.26112G>C
NG_027988.2:g.26112G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698506.1:c.-47-5691G>C	ENSP00000513758.1:n.-47-5691G>C
ENST00000359321.2:c.121+5647G>C MANE Select	ENSP00000352271.1:n.121+5647G>C
ENST00000359321.1:c.121+5647G>C	ENSP00000352271.1:n.121+5647G>C
ENST00000495707.1:n.143+5647G>C
NM_005431.1:c.121+5647G>C	NP_005422.1:n.121+5647G>C
NM_005431.2:c.121+5647G>C MANE Select	NP_005422.1:n.121+5647G>C