Canonical Allele Identifier: CA507741037

Gene: XRCC1

Linked Data

• dbSNP Id: rs960861282
• gnomAD v4: 19-43551627-C-G
• MyVariant Identifiers: chr19:g.44055779C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43551627C>G , CM000681.2:g.43551627C>G	GRCh38
NC_000019.9:g.44055779C>G , CM000681.1:g.44055779C>G	GRCh37
NC_000019.8:g.48747619C>G	NCBI36
NG_033799.1:g.28952G>C , LRG_784:g.28952G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262887.10:c.1143G>C MANE Select	ENSP00000262887.5:p.Val381=
ENST00000262887.9:c.1143G>C	ENSP00000262887.4:p.Val381=
ENST00000543982.5:c.1050G>C	ENSP00000443671.1:p.Val350=
ENST00000597811.5:c.753G>C
NM_006297.2:c.1143G>C , LRG_784t1:c.1143G>C	NP_006288.2:p.Val381=
NM_006297.3:c.1143G>C MANE Select	NP_006288.2:p.Val381=