Canonical Allele Identifier: CA370199525

Gene: XRCC2

Linked Data

• MyVariant Identifiers: chr7:g.152357848C>A (hg19) ; chr7:g.152660763C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152660763C>A , CM000669.2:g.152660763C>A	GRCh38
NC_000007.13:g.152357848C>A , CM000669.1:g.152357848C>A	GRCh37
NC_000007.12:g.151988781C>A	NCBI36
NG_027988.1:g.20403G>T
NG_027988.2:g.20403G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.-47-11400G>T	ENSP00000513758.1:n.-47-11400G>T
ENST00000698507.1:n.127G>T
ENST00000359321.2:c.59G>T MANE Select	ENSP00000352271.1:p.Gly20Val
ENST00000359321.1:c.59G>T	ENSP00000352271.1:p.Gly20Val
ENST00000495707.1:n.81G>T
NM_005431.1:c.59G>T	NP_005422.1:p.Gly20Val
NM_005431.2:c.59G>T MANE Select	NP_005422.1:p.Gly20Val