Canonical Allele Identifier: CA406203668
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs2146049241
MyVariant Identifiers: chr19:g.44055831A>G (hg19) chr19:g.43551679A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551679A>G , CM000681.2:g.43551679A>G GRCh38
NC_000019.9:g.44055831A>G , CM000681.1:g.44055831A>G GRCh37
NC_000019.8:g.48747671A>G NCBI36
NG_033799.1:g.28900T>C , LRG_784:g.28900T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1091T>C MANE Select ENSP00000262887.5:p.Phe364Ser
ENST00000262887.9:c.1091T>C ENSP00000262887.4:p.Phe364Ser
ENST00000543982.5:c.998T>C ENSP00000443671.1:p.Phe333Ser
ENST00000597811.5:c.701T>C
NM_006297.2:c.1091T>C , LRG_784t1:c.1091T>C NP_006288.2:p.Phe364Ser
NM_006297.3:c.1091T>C MANE Select NP_006288.2:p.Phe364Ser
Search 100 bp 5'
Search 100 bp 3'