Linked Data
dbSNP Id:
rs2136770731
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.110913235A>C , CM000674.2:g.110913235A>C | GRCh38 |
| NC_000012.11:g.111351039A>C , CM000674.1:g.111351039A>C | GRCh37 |
| NC_000012.10:g.109835422A>C | NCBI36 |
| NG_007554.1:g.12343T>G , LRG_393:g.12343T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000228841.15:c.353+11T>G MANE Select | ENSP00000228841.8:n.353+11T>G | |
| ENST00000663220.1:c.296+11T>G | ENSP00000499568.1:n.296+11T>G | |
| ENST00000228841.12:c.353+11T>G | ENSP00000228841.7:n.353+11T>G | |
| ENST00000548438.1:c.311+11T>G | ENSP00000447154.1:n.311+11T>G | |
| ENST00000549029.1:n.195T>G | ||
| NM_000432.3:c.353+11T>G , LRG_393t1:c.353+11T>G | NP_000423.2:n.353+11T>G | |
| NM_000432.4:c.353+11T>G MANE Select | NP_000423.2:n.353+11T>G |