Canonical Allele Identifier: CA370198008

Gene: XRCC2

Linked Data

• MyVariant Identifiers: chr7:g.152345814T>A (hg19) ; chr7:g.152648729T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152648729T>A , CM000669.2:g.152648729T>A	GRCh38
NC_000007.13:g.152345814T>A , CM000669.1:g.152345814T>A	GRCh37
NC_000007.12:g.151976747T>A	NCBI36
NG_027988.1:g.32437A>T
NG_027988.2:g.32437A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.588A>T	ENSP00000513758.1:p.Gln196His
ENST00000359321.2:c.756A>T MANE Select	ENSP00000352271.1:p.Gln252His
ENST00000359321.1:c.756A>T	ENSP00000352271.1:p.Gln252His
ENST00000495707.1:n.778A>T
NM_005431.1:c.756A>T	NP_005422.1:p.Gln252His
NM_005431.2:c.756A>T MANE Select	NP_005422.1:p.Gln252His