Canonical Allele Identifier: CA633476308

Gene: XRCC1

Linked Data

• dbSNP Id: rs935284344
• gnomAD v2: 19-44055914-G-C
• gnomAD v3: 19-43551762-G-C
• gnomAD v4: 19-43551762-G-C
• MyVariant Identifiers: chr19:g.44055914G>C (hg19) ; chr19:g.43551762G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43551762G>C , CM000681.2:g.43551762G>C	GRCh38
NC_000019.9:g.44055914G>C , CM000681.1:g.44055914G>C	GRCh37
NC_000019.8:g.48747754G>C	NCBI36
NG_033799.1:g.28817C>G , LRG_784:g.28817C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262887.10:c.1083-75C>G MANE Select	ENSP00000262887.5:n.1083-75C>G
ENST00000262887.9:c.1083-75C>G	ENSP00000262887.4:n.1083-75C>G
ENST00000543982.5:c.990-75C>G	ENSP00000443671.1:n.990-75C>G
ENST00000597811.5:c.693-75C>G
NM_006297.2:c.1083-75C>G , LRG_784t1:c.1083-75C>G	NP_006288.2:n.1083-75C>G
NM_006297.3:c.1083-75C>G MANE Select	NP_006288.2:n.1083-75C>G