Linked Data
dbSNP Id:
rs1768158475
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32819202T>A , CM000668.2:g.32819202T>A | GRCh38 |
| NC_000006.11:g.32786979T>A , CM000668.1:g.32786979T>A | GRCh37 |
| NC_000006.10:g.32894957T>A | NCBI36 |
| NG_009793.3:g.24569A>T | |
| NG_012008.1:g.2847A>T | |
| NG_009793.4:g.24569A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648009.1:c.-2+1109A>T | ENSP00000496848.1:n.-2+1109A>T | |
| ENST00000452392.2:c.1933-2250A>T | ENSP00000391806.2:n.1933-2250A>T |