Canonical Allele Identifier: CA633476259
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs1429371977
gnomAD v2: 19-44056038-G-A
gnomAD v3: 19-43551886-G-A
gnomAD v4: 19-43551886-G-A
MyVariant Identifiers: chr19:g.44056038G>A (hg19) chr19:g.43551886G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551886G>A , CM000681.2:g.43551886G>A GRCh38
NC_000019.9:g.44056038G>A , CM000681.1:g.44056038G>A GRCh37
NC_000019.8:g.48747878G>A NCBI36
NG_033799.1:g.28693C>T , LRG_784:g.28693C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1082+131C>T MANE Select ENSP00000262887.5:n.1082+131C>T
ENST00000262887.9:c.1082+131C>T ENSP00000262887.4:n.1082+131C>T
ENST00000543982.5:c.989+131C>T ENSP00000443671.1:n.989+131C>T
ENST00000597811.5:c.692+131C>T
NM_006297.2:c.1082+131C>T , LRG_784t1:c.1082+131C>T NP_006288.2:n.1082+131C>T
NM_006297.3:c.1082+131C>T MANE Select NP_006288.2:n.1082+131C>T
Search 100 bp 5'
Search 100 bp 3'