Linked Data
dbSNP Id:
rs215659
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.32337239A>G , CM000669.2:g.32337239A>G | GRCh38 |
| NC_000007.13:g.32376851A>G , CM000669.1:g.32376851A>G | GRCh37 |
| NC_000007.12:g.32343376A>G | NCBI36 |
| NG_051183.1:g.95986T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000672256.1:c.310+90583T>C | ENSP00000499831.1:n.310+90583T>C | |
| NM_001322059.1:c.310+90583T>C | NP_001308988.1:n.310+90583T>C | |
| NM_001322059.2:c.310+90583T>C | NP_001308988.1:n.310+90583T>C |