Canonical Allele Identifier: CA370198694
Gene: XRCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.152346131T>G (hg19) chr7:g.152649046T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152649046T>G , CM000669.2:g.152649046T>G GRCh38
NC_000007.13:g.152346131T>G , CM000669.1:g.152346131T>G GRCh37
NC_000007.12:g.151977064T>G NCBI36
NG_027988.1:g.32120A>C
NG_027988.2:g.32120A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.271A>C ENSP00000513758.1:p.Ile91Leu
ENST00000359321.2:c.439A>C MANE Select ENSP00000352271.1:p.Ile147Leu
ENST00000359321.1:c.439A>C ENSP00000352271.1:p.Ile147Leu
ENST00000495707.1:n.461A>C
NM_005431.1:c.439A>C NP_005422.1:p.Ile147Leu
NM_005431.2:c.439A>C MANE Select NP_005422.1:p.Ile147Leu
Search 100 bp 5'
Search 100 bp 3'