Canonical Allele Identifier: CA835376746
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1416050233
gnomAD v3: 7-152648425-AAAAG-A
gnomAD v4: 7-152648425-AAAAG-A
MyVariant Identifiers: chr7:g.152345511_152345514del (hg19) chr7:g.152648426_152648429del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648429_152648432del , CM000669.2:g.152648429_152648432del GRCh38
NC_000007.13:g.152345514_152345517del , CM000669.1:g.152345514_152345517del GRCh37
NC_000007.12:g.151976447_151976450del NCBI36
NG_027988.1:g.32737_32740del
NG_027988.2:g.32737_32740del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*213_*216del ENSP00000513758.1:n.*213_*216del
ENST00000359321.2:c.*213_*216del MANE Select ENSP00000352271.1:n.*213_*216del
ENST00000359321.1:c.*213_*216del ENSP00000352271.1:n.*213_*216del
ENST00000495707.1:n.1078_1081del
NM_005431.1:c.*213_*216del NP_005422.1:n.*213_*216del
NM_005431.2:c.*213_*216del MANE Select NP_005422.1:n.*213_*216del
Search 100 bp 5'
Search 100 bp 3'