Canonical Allele Identifier: CA370199629

Gene: XRCC2

Linked Data

• MyVariant Identifiers: chr7:g.152373154G>A (hg19) ; chr7:g.152676069G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152676069G>A , CM000669.2:g.152676069G>A	GRCh38
NC_000007.13:g.152373154G>A , CM000669.1:g.152373154G>A	GRCh37
NC_000007.12:g.152004087G>A	NCBI36
NG_027988.1:g.5097C>T
NG_027988.2:g.5097C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.-76C>T	ENSP00000513758.1:n.-76C>T
ENST00000698507.1:n.79C>T
ENST00000359321.2:c.11C>T MANE Select	ENSP00000352271.1:p.Ala4Val
ENST00000359321.1:c.11C>T	ENSP00000352271.1:p.Ala4Val
NM_005431.1:c.11C>T	NP_005422.1:p.Ala4Val
NM_005431.2:c.11C>T MANE Select	NP_005422.1:p.Ala4Val