Linked Data
dbSNP Id:
rs1679916608
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.27323116C>T , CM000664.2:g.27323116C>T | GRCh38 |
| NC_000002.11:g.27545983C>T , CM000664.1:g.27545983C>T | GRCh37 |
| NC_000002.10:g.27399487C>T | NCBI36 |
| NG_008075.1:g.4449G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357186.10:c.18+1317G>A | ENSP00000349713.6:n.18+1317G>A | |
| XM_005264327.2:c.-194G>A | XP_005264384.1:n.-194G>A |