Canonical Allele Identifier: CA882544377
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs1261550755
gnomAD v4: 19-43551764-C-G
MyVariant Identifiers: chr19:g.44055916C>G (hg19) chr19:g.43551764C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551764C>G , CM000681.2:g.43551764C>G GRCh38
NC_000019.9:g.44055916C>G , CM000681.1:g.44055916C>G GRCh37
NC_000019.8:g.48747756C>G NCBI36
NG_033799.1:g.28815G>C , LRG_784:g.28815G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1083-77G>C MANE Select ENSP00000262887.5:n.1083-77G>C
ENST00000262887.9:c.1083-77G>C ENSP00000262887.4:n.1083-77G>C
ENST00000543982.5:c.990-77G>C ENSP00000443671.1:n.990-77G>C
ENST00000597811.5:c.693-77G>C
NM_006297.2:c.1083-77G>C , LRG_784t1:c.1083-77G>C NP_006288.2:n.1083-77G>C
NM_006297.3:c.1083-77G>C MANE Select NP_006288.2:n.1083-77G>C
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