Linked Data
dbSNP Id:
rs9260200
gnomAD v2:
6-29912657-C-T
gnomAD v3:
6-29944880-C-T
gnomAD v4:
6-29944880-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29944880C>T , CM000668.2:g.29944880C>T | GRCh38 |
| NC_000006.11:g.29912657C>T , CM000668.1:g.29912657C>T | GRCh37 |
| NC_000006.10:g.30020636C>T | NCBI36 |
| NG_029217.2:g.7416C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000638375.2:c.896-179C>T | ENSP00000492789.2:n.896-179C>T | |
| ENST00000706892.1:n.2232C>T | ||
| ENST00000706893.1:c.1065-179C>T | ENSP00000516609.1:n.1065-179C>T | |
| ENST00000706894.1:c.1013-179C>T | ENSP00000516610.1:n.1013-179C>T | |
| ENST00000706895.1:n.1654C>T | ||
| ENST00000706896.1:n.2130C>T | ||
| ENST00000706897.1:n.1552C>T | ||
| ENST00000706898.1:c.1031-179C>T | ENSP00000516611.1:n.1031-179C>T | |
| ENST00000706899.1:n.1867-179C>T | ||
| ENST00000706900.1:c.929-179C>T | ENSP00000516617.1:n.929-179C>T | |
| ENST00000706901.1:c.1013-179C>T | ENSP00000516612.1:n.1013-179C>T | |
| ENST00000706902.1:c.1013-179C>T | ENSP00000516613.1:n.1013-179C>T | |
| ENST00000706903.1:c.1013-179C>T | ENSP00000516614.1:n.1013-179C>T | |
| ENST00000706904.1:c.1013-179C>T | ENSP00000516615.1:n.1013-179C>T | |
| ENST00000706905.1:c.1013-179C>T | ENSP00000516616.1:n.1013-179C>T | |
| ENST00000376809.10:c.1013-179C>T MANE Select | ENSP00000366005.5:n.1013-179C>T | |
| ENST00000638375.1:c.896-179C>T | ENSP00000492789.1:n.896-179C>T | |
| ENST00000376802.2:c.895+483C>T | ENSP00000365998.2:n.895+483C>T | |
| ENST00000376806.9:c.1031-179C>T | ENSP00000366002.5:n.1031-179C>T | |
| ENST00000376809.9:c.1013-179C>T | ENSP00000366005.5:n.1013-179C>T | |
| ENST00000396634.5:c.1013-179C>T | ENSP00000379873.1:n.1013-179C>T | |
| ENST00000461903.1:n.1272-179C>T | ||
| ENST00000479320.5:n.1254-179C>T | ||
| ENST00000495183.5:n.1256-183C>T | ||
| ENST00000496081.5:n.1093C>T | ||
| NM_002116.7:c.1013-179C>T | NP_002107.3:n.1013-179C>T | |
| NM_002116.8:c.1013-179C>T MANE Select | NP_002107.3:n.1013-179C>T |