Linked Data
dbSNP Id:
rs485499
gnomAD v2:
3-159745863-T-C
gnomAD v3:
3-160028076-T-C
gnomAD v4:
3-160028076-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.160028076T>C , CM000665.2:g.160028076T>C | GRCh38 |
| NC_000003.11:g.159745863T>C , CM000665.1:g.159745863T>C | GRCh37 |
| NC_000003.10:g.161228557T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_104132.1:n.373+1190T>C (LINC01100) | ||
| NR_108088.1:n.518-2542A>G (IL12A-AS1) |