Linked Data
dbSNP Id:
rs769263687
ExAC:
6:29910489 G / T
gnomAD v2:
6-29910489-G-T
gnomAD v3:
6-29942712-G-T
gnomAD v4:
6-29942712-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29942712G>T , CM000668.2:g.29942712G>T | GRCh38 |
| NC_000006.11:g.29910489G>T , CM000668.1:g.29910489G>T | GRCh37 |
| NC_000006.10:g.30018468G>T | NCBI36 |
| NG_029217.2:g.5247G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000638375.2:c.74-45G>T | ENSP00000492789.2:n.74-45G>T | |
| ENST00000706892.1:n.350-45G>T | ||
| ENST00000706893.1:c.74-45G>T | ENSP00000516609.1:n.74-45G>T | |
| ENST00000706894.1:c.74-45G>T | ENSP00000516610.1:n.74-45G>T | |
| ENST00000706895.1:n.350-45G>T | ||
| ENST00000706896.1:n.350-45G>T | ||
| ENST00000706897.1:n.350-45G>T | ||
| ENST00000706898.1:c.74-45G>T | ENSP00000516611.1:n.74-45G>T | |
| ENST00000706899.1:n.350-45G>T | ||
| ENST00000706901.1:c.74-45G>T | ENSP00000516612.1:n.74-45G>T | |
| ENST00000706902.1:c.74-45G>T | ENSP00000516613.1:n.74-45G>T | |
| ENST00000706903.1:c.74-45G>T | ENSP00000516614.1:n.74-45G>T | |
| ENST00000706904.1:c.74-45G>T | ENSP00000516615.1:n.74-45G>T | |
| ENST00000706905.1:c.74-45G>T | ENSP00000516616.1:n.74-45G>T | |
| ENST00000376809.10:c.74-45G>T MANE Select | ENSP00000366005.5:n.74-45G>T | |
| ENST00000638375.1:c.74-45G>T | ENSP00000492789.1:n.74-45G>T | |
| ENST00000376802.2:c.74-45G>T | ENSP00000365998.2:n.74-45G>T | |
| ENST00000376806.9:c.74-45G>T | ENSP00000366002.5:n.74-45G>T | |
| ENST00000376809.9:c.74-45G>T | ENSP00000366005.5:n.74-45G>T | |
| ENST00000396634.5:c.74-45G>T | ENSP00000379873.1:n.74-45G>T | |
| ENST00000429656.1:n.356C>A | ||
| ENST00000461903.1:n.74-45G>T | ||
| ENST00000479320.5:n.74-45G>T | ||
| ENST00000495183.5:n.76-45G>T | ||
| ENST00000496081.5:n.80-45G>T | ||
| NM_002116.7:c.74-45G>T | NP_002107.3:n.74-45G>T | |
| NM_002116.8:c.74-45G>T MANE Select | NP_002107.3:n.74-45G>T |