Canonical Allele Identifier: CA507741045
Gene: XRCC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.44055791T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551639T>C , CM000681.2:g.43551639T>C GRCh38
NC_000019.9:g.44055791T>C , CM000681.1:g.44055791T>C GRCh37
NC_000019.8:g.48747631T>C NCBI36
NG_033799.1:g.28940A>G , LRG_784:g.28940A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1131A>G MANE Select ENSP00000262887.5:p.Gly377=
ENST00000262887.9:c.1131A>G ENSP00000262887.4:p.Gly377=
ENST00000543982.5:c.1038A>G ENSP00000443671.1:p.Gly346=
ENST00000597811.5:c.741A>G
NM_006297.2:c.1131A>G , LRG_784t1:c.1131A>G NP_006288.2:p.Gly377=
NM_006297.3:c.1131A>G MANE Select NP_006288.2:p.Gly377=