Linked Data
dbSNP Id:
rs1598044446
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58281404C>T , CM000679.2:g.58281404C>T | GRCh38 |
| NC_000017.10:g.56358765C>T , CM000679.1:g.56358765C>T | GRCh37 |
| NC_000017.9:g.53713764C>T | NCBI36 |
| NG_009629.1:g.4532G>A , LRG_84:g.4532G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_011524821.1:c.71-335G>A | XP_011523123.1:n.71-335G>A | |
| XM_011524823.1:c.71-335G>A | XP_011523125.1:n.71-335G>A |