Canonical Allele Identifier: CA370198033
Gene: XRCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.152345824C>T (hg19) chr7:g.152648739C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648739C>T , CM000669.2:g.152648739C>T GRCh38
NC_000007.13:g.152345824C>T , CM000669.1:g.152345824C>T GRCh37
NC_000007.12:g.151976757C>T NCBI36
NG_027988.1:g.32427G>A
NG_027988.2:g.32427G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.578G>A ENSP00000513758.1:p.Ser193Asn
ENST00000359321.2:c.746G>A MANE Select ENSP00000352271.1:p.Ser249Asn
ENST00000359321.1:c.746G>A ENSP00000352271.1:p.Ser249Asn
ENST00000495707.1:n.768G>A
NM_005431.1:c.746G>A NP_005422.1:p.Ser249Asn
NM_005431.2:c.746G>A MANE Select NP_005422.1:p.Ser249Asn
Search 100 bp 5'
Search 100 bp 3'