Canonical Allele Identifier: CA9488526
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs779934492
ExAC: 19:44055750 C / T
gnomAD v2: 19-44055750-C-T
gnomAD v4: 19-43551598-C-T
MyVariant Identifiers: chr19:g.44055750C>T (hg19) chr19:g.43551598C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551598C>T , CM000681.2:g.43551598C>T GRCh38
NC_000019.9:g.44055750C>T , CM000681.1:g.44055750C>T GRCh37
NC_000019.8:g.48747590C>T NCBI36
NG_033799.1:g.28981G>A , LRG_784:g.28981G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1172G>A MANE Select ENSP00000262887.5:p.Arg391His
ENST00000262887.9:c.1172G>A ENSP00000262887.4:p.Arg391His
ENST00000543982.5:c.1079G>A ENSP00000443671.1:p.Arg360His
ENST00000597811.5:c.782G>A
NM_006297.2:c.1172G>A , LRG_784t1:c.1172G>A NP_006288.2:p.Arg391His
NM_006297.3:c.1172G>A MANE Select NP_006288.2:p.Arg391His
Search 100 bp 5'
Search 100 bp 3'