Canonical Allele Identifier: CA406203283
Gene: XRCC1 HGNC NCBI

Linked Data

COSMIC: COSM5056724
MyVariant Identifiers: chr19:g.44055753T>C (hg19) chr19:g.43551601T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551601T>C , CM000681.2:g.43551601T>C GRCh38
NC_000019.9:g.44055753T>C , CM000681.1:g.44055753T>C GRCh37
NC_000019.8:g.48747593T>C NCBI36
NG_033799.1:g.28978A>G , LRG_784:g.28978A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1169A>G MANE Select ENSP00000262887.5:p.His390Arg
ENST00000262887.9:c.1169A>G ENSP00000262887.4:p.His390Arg
ENST00000543982.5:c.1076A>G ENSP00000443671.1:p.His359Arg
ENST00000597811.5:c.779A>G
NM_006297.2:c.1169A>G , LRG_784t1:c.1169A>G NP_006288.2:p.His390Arg
NM_006297.3:c.1169A>G MANE Select NP_006288.2:p.His390Arg
Search 100 bp 5'
Search 100 bp 3'