Canonical Allele Identifier: CA835365654
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1449695755
MyVariant Identifiers: chr7:g.152373120_152373121insC (hg19) chr7:g.152676035_152676036insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676036dup , CM000669.2:g.152676036dup GRCh38
NC_000007.13:g.152373121dup , CM000669.1:g.152373121dup GRCh37
NC_000007.12:g.152004054dup NCBI36
NG_027988.1:g.5130dup
NG_027988.2:g.5130dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-48+5dup ENSP00000513758.1:n.-48+5dup
ENST00000698507.1:n.107+5dup
ENST00000359321.2:c.39+5dup MANE Select ENSP00000352271.1:n.39+5dup
ENST00000359321.1:c.39+5dup ENSP00000352271.1:n.39+5dup
NM_005431.1:c.39+5dup NP_005422.1:n.39+5dup
NM_005431.2:c.39+5dup MANE Select NP_005422.1:n.39+5dup
Search 100 bp 5'
Search 100 bp 3'