Linked Data
dbSNP Id:
rs1357289736
gnomAD v2:
6-29912443-G-A
gnomAD v3:
6-29944666-G-A
gnomAD v4:
6-29944666-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29944666G>A , CM000668.2:g.29944666G>A | GRCh38 |
| NC_000006.11:g.29912443G>A , CM000668.1:g.29912443G>A | GRCh37 |
| NC_000006.10:g.30020422G>A | NCBI36 |
| NG_029217.2:g.7202G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000638375.2:c.895+269G>A | ENSP00000492789.2:n.895+269G>A | |
| ENST00000706892.1:n.2018G>A | ||
| ENST00000706893.1:c.1064+32G>A | ENSP00000516609.1:n.1064+32G>A | |
| ENST00000706894.1:c.1012+50G>A | ENSP00000516610.1:n.1012+50G>A | |
| ENST00000706895.1:n.1440G>A | ||
| ENST00000706896.1:n.1916G>A | ||
| ENST00000706897.1:n.1338G>A | ||
| ENST00000706898.1:c.1030+32G>A | ENSP00000516611.1:n.1030+32G>A | |
| ENST00000706899.1:n.1866+50G>A | ||
| ENST00000706900.1:c.928+50G>A | ENSP00000516617.1:n.928+50G>A | |
| ENST00000706901.1:c.1012+50G>A | ENSP00000516612.1:n.1012+50G>A | |
| ENST00000706902.1:c.1012+50G>A | ENSP00000516613.1:n.1012+50G>A | |
| ENST00000706903.1:c.1012+50G>A | ENSP00000516614.1:n.1012+50G>A | |
| ENST00000706904.1:c.1012+50G>A | ENSP00000516615.1:n.1012+50G>A | |
| ENST00000706905.1:c.1012+50G>A | ENSP00000516616.1:n.1012+50G>A | |
| ENST00000376809.10:c.1012+50G>A MANE Select | ENSP00000366005.5:n.1012+50G>A | |
| ENST00000638375.1:c.895+269G>A | ENSP00000492789.1:n.895+269G>A | |
| ENST00000376802.2:c.895+269G>A | ENSP00000365998.2:n.895+269G>A | |
| ENST00000376806.9:c.1030+32G>A | ENSP00000366002.5:n.1030+32G>A | |
| ENST00000376809.9:c.1012+50G>A | ENSP00000366005.5:n.1012+50G>A | |
| ENST00000396634.5:c.1012+50G>A | ENSP00000379873.1:n.1012+50G>A | |
| ENST00000461903.1:n.1271+32G>A | ||
| ENST00000479320.5:n.1253+50G>A | ||
| ENST00000495183.5:n.1255+50G>A | ||
| ENST00000496081.5:n.879G>A | ||
| NM_002116.7:c.1012+50G>A | NP_002107.3:n.1012+50G>A | |
| NM_002116.8:c.1012+50G>A MANE Select | NP_002107.3:n.1012+50G>A |