Linked Data
dbSNP Id:
rs564312430
ExAC:
1:103444570 A / C
gnomAD v2:
1-103444570-A-C
gnomAD v4:
1-102979014-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.102979014A>C , CM000663.2:g.102979014A>C | GRCh38 |
| NC_000001.10:g.103444570A>C , CM000663.1:g.103444570A>C | GRCh37 |
| NC_000001.9:g.103217158A>C | NCBI36 |
| NG_008033.1:g.134483T>G | |
| NG_008033.2:g.134483T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370096.9:c.2655+46T>G MANE Select | ENSP00000359114.3:n.2655+46T>G | |
| ENST00000353414.8:c.2538+46T>G | ENSP00000302551.6:n.2538+46T>G | |
| ENST00000358392.6:c.2691+46T>G | ENSP00000351163.2:n.2691+46T>G | |
| ENST00000370096.7:c.2655+46T>G | ENSP00000359114.3:n.2655+46T>G | |
| ENST00000512756.5:c.2307+46T>G | ENSP00000426533.1:n.2307+46T>G | |
| ENST00000635193.1:c.1989+46T>G | ||
| NM_001190709.1:c.2538+46T>G | NP_001177638.1:n.2538+46T>G | |
| NM_001854.3:c.2655+46T>G | NP_001845.3:n.2655+46T>G | |
| NM_080629.2:c.2691+46T>G | NP_542196.2:n.2691+46T>G | |
| NM_080630.3:c.2307+46T>G | NP_542197.3:n.2307+46T>G | |
| XM_011540719.1:c.2655+46T>G | XP_011539021.1:n.2655+46T>G | |
| XM_011540720.1:c.888+46T>G | XP_011539022.1:n.888+46T>G | |
| XM_011540721.1:c.243+46T>G | XP_011539023.1:n.243+46T>G | |
| XR_946545.1:n.3069+46T>G | ||
| NR_134980.1:n.2989+46T>G | ||
| XM_017000334.1:c.2808+46T>G | XP_016855823.1:n.2808+46T>G | |
| XM_017000335.1:c.2802+46T>G | XP_016855824.1:n.2802+46T>G | |
| XM_017000336.1:c.2808+46T>G | XP_016855825.1:n.2808+46T>G | |
| XM_017000337.1:c.1206+46T>G | XP_016855826.1:n.1206+46T>G | |
| NM_001854.4:c.2655+46T>G MANE Select | NP_001845.3:n.2655+46T>G | |
| NM_080630.4:c.2307+46T>G | NP_542197.3:n.2307+46T>G | |
| NR_134980.2:n.3015+46T>G | ||
| NM_001190709.2:c.2538+46T>G | NP_001177638.1:n.2538+46T>G | |
| NM_080629.3:c.2691+46T>G | NP_542196.2:n.2691+46T>G |