Canonical Allele Identifier: CA2337551212
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs1972573338
gnomAD v4: 19-43551473-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551473C>T , CM000681.2:g.43551473C>T GRCh38
NC_000019.9:g.44055625C>T , CM000681.1:g.44055625C>T GRCh37
NC_000019.8:g.48747465C>T NCBI36
NG_033799.1:g.29106G>A , LRG_784:g.29106G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1199+98G>A MANE Select ENSP00000262887.5:n.1199+98G>A
ENST00000262887.9:c.1199+98G>A ENSP00000262887.4:n.1199+98G>A
ENST00000543982.5:c.1106+98G>A ENSP00000443671.1:n.1106+98G>A
NM_006297.2:c.1199+98G>A , LRG_784t1:c.1199+98G>A NP_006288.2:n.1199+98G>A
NM_006297.3:c.1199+98G>A MANE Select NP_006288.2:n.1199+98G>A
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