Linked Data
dbSNP Id:
rs1679923087
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.27323194C>A , CM000664.2:g.27323194C>A | GRCh38 |
| NC_000002.11:g.27546061C>A , CM000664.1:g.27546061C>A | GRCh37 |
| NC_000002.10:g.27399565C>A | NCBI36 |
| NG_008075.1:g.4371G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357186.10:c.18+1239G>T | ENSP00000349713.6:n.18+1239G>T | |
| XM_005264327.2:c.-272G>T | XP_005264384.1:n.-272G>T |