Linked Data
dbSNP Id:
rs1755114254
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149981899G>T , CM000667.2:g.149981899G>T | GRCh38 |
| NC_000005.9:g.149361462G>T , CM000667.1:g.149361462G>T | GRCh37 |
| NC_000005.8:g.149341655G>T | NCBI36 |
| NG_007147.2:g.23017G>T , LRG_684:g.23017G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286298.5:c.*86G>T MANE Select | ENSP00000286298.4:n.*86G>T | |
| ENST00000286298.4:c.*86G>T | ENSP00000286298.4:n.*86G>T | |
| ENST00000503336.1:c.372+3548G>T | ENSP00000426053.1:n.372+3548G>T | |
| NM_000112.3:c.*86G>T , LRG_684t1:c.*86G>T | NP_000103.2:n.*86G>T | |
| XM_017009191.2:c.*13-30G>T | XP_016864680.1:n.*13-30G>T | |
| NM_000112.4:c.*86G>T MANE Select | NP_000103.2:n.*86G>T |