Canonical Allele Identifier: CA507741181
Gene: XRCC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.44056315G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43552163G>T , CM000681.2:g.43552163G>T GRCh38
NC_000019.9:g.44056315G>T , CM000681.1:g.44056315G>T GRCh37
NC_000019.8:g.48748155G>T NCBI36
NG_033799.1:g.28416C>A , LRG_784:g.28416C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.936C>A MANE Select ENSP00000262887.5:p.Gly312=
ENST00000262887.9:c.936C>A ENSP00000262887.4:p.Gly312=
ENST00000543982.5:c.843C>A ENSP00000443671.1:p.Gly281=
ENST00000595789.5:n.1057C>A
ENST00000597811.5:c.546C>A
ENST00000598422.1:n.616C>A
NM_006297.2:c.936C>A , LRG_784t1:c.936C>A NP_006288.2:p.Gly312=
NM_006297.3:c.936C>A MANE Select NP_006288.2:p.Gly312=