Canonical Allele Identifier: CA2337551418
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs1972579287
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551866G>C , CM000681.2:g.43551866G>C GRCh38
NC_000019.9:g.44056018G>C , CM000681.1:g.44056018G>C GRCh37
NC_000019.8:g.48747858G>C NCBI36
NG_033799.1:g.28713C>G , LRG_784:g.28713C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1082+151C>G MANE Select ENSP00000262887.5:n.1082+151C>G
ENST00000262887.9:c.1082+151C>G ENSP00000262887.4:n.1082+151C>G
ENST00000543982.5:c.989+151C>G ENSP00000443671.1:n.989+151C>G
ENST00000597811.5:c.692+151C>G
NM_006297.2:c.1082+151C>G , LRG_784t1:c.1082+151C>G NP_006288.2:n.1082+151C>G
NM_006297.3:c.1082+151C>G MANE Select NP_006288.2:n.1082+151C>G
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