Canonical Allele Identifier: CA507741047
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs761583025
MyVariant Identifiers: chr19:g.44055794C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551642C>A , CM000681.2:g.43551642C>A GRCh38
NC_000019.9:g.44055794C>A , CM000681.1:g.44055794C>A GRCh37
NC_000019.8:g.48747634C>A NCBI36
NG_033799.1:g.28937G>T , LRG_784:g.28937G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1128G>T MANE Select ENSP00000262887.5:p.Leu376=
ENST00000262887.9:c.1128G>T ENSP00000262887.4:p.Leu376=
ENST00000543982.5:c.1035G>T ENSP00000443671.1:p.Leu345=
ENST00000597811.5:c.738G>T
NM_006297.2:c.1128G>T , LRG_784t1:c.1128G>T NP_006288.2:p.Leu376=
NM_006297.3:c.1128G>T MANE Select NP_006288.2:p.Leu376=