Canonical Allele Identifier: CA370198027
Gene: XRCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.152345821C>T (hg19) chr7:g.152648736C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648736C>T , CM000669.2:g.152648736C>T GRCh38
NC_000007.13:g.152345821C>T , CM000669.1:g.152345821C>T GRCh37
NC_000007.12:g.151976754C>T NCBI36
NG_027988.1:g.32430G>A
NG_027988.2:g.32430G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.581G>A ENSP00000513758.1:p.Ser194Asn
ENST00000359321.2:c.749G>A MANE Select ENSP00000352271.1:p.Ser250Asn
ENST00000359321.1:c.749G>A ENSP00000352271.1:p.Ser250Asn
ENST00000495707.1:n.771G>A
NM_005431.1:c.749G>A NP_005422.1:p.Ser250Asn
NM_005431.2:c.749G>A MANE Select NP_005422.1:p.Ser250Asn
Search 100 bp 5'
Search 100 bp 3'