Canonical Allele Identifier: CA406204976
Gene: XRCC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.44056323G>C (hg19) chr19:g.43552171G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43552171G>C , CM000681.2:g.43552171G>C GRCh38
NC_000019.9:g.44056323G>C , CM000681.1:g.44056323G>C GRCh37
NC_000019.8:g.48748163G>C NCBI36
NG_033799.1:g.28408C>G , LRG_784:g.28408C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.928C>G MANE Select ENSP00000262887.5:p.Arg310Gly
ENST00000262887.9:c.928C>G ENSP00000262887.4:p.Arg310Gly
ENST00000543982.5:c.835C>G ENSP00000443671.1:p.Arg279Gly
ENST00000595789.5:n.1049C>G
ENST00000597811.5:c.538C>G
ENST00000598422.1:n.608C>G
NM_006297.2:c.928C>G , LRG_784t1:c.928C>G NP_006288.2:p.Arg310Gly
NM_006297.3:c.928C>G MANE Select NP_006288.2:p.Arg310Gly
Search 100 bp 5'
Search 100 bp 3'