Canonical Allele Identifier:
CA1458504871
Gene:
Linked Data
dbSNP Id:
rs1720487404
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.54228537G>T , CM000666.2:g.54228537G>T | GRCh38 |
| NC_000004.11:g.55094704G>T , CM000666.1:g.55094704G>T | GRCh37 |
| NC_000004.10:g.54789461G>T | NCBI36 |
| NG_009250.1:g.4441G>T , LRG_309:g.4441G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000507166.5:c.1018-46388G>T | ENSP00000423325.1:n.1018-46388G>T |