Canonical Allele Identifier: CA9488527
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs747185141
ExAC: 19:44055751 G / A
gnomAD v2: 19-44055751-G-A
gnomAD v3: 19-43551599-G-A
gnomAD v4: 19-43551599-G-A
COSMIC: COSM300455
MyVariant Identifiers: chr19:g.44055751G>A (hg19) chr19:g.43551599G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551599G>A , CM000681.2:g.43551599G>A GRCh38
NC_000019.9:g.44055751G>A , CM000681.1:g.44055751G>A GRCh37
NC_000019.8:g.48747591G>A NCBI36
NG_033799.1:g.28980C>T , LRG_784:g.28980C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1171C>T MANE Select ENSP00000262887.5:p.Arg391Cys
ENST00000262887.9:c.1171C>T ENSP00000262887.4:p.Arg391Cys
ENST00000543982.5:c.1078C>T ENSP00000443671.1:p.Arg360Cys
ENST00000597811.5:c.781C>T
NM_006297.2:c.1171C>T , LRG_784t1:c.1171C>T NP_006288.2:p.Arg391Cys
NM_006297.3:c.1171C>T MANE Select NP_006288.2:p.Arg391Cys
Search 100 bp 5'
Search 100 bp 3'