Linked Data
dbSNP Id:
rs766511805
ExAC:
1:103444275 G / C
gnomAD v2:
1-103444275-G-C
gnomAD v4:
1-102978719-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.102978719G>C , CM000663.2:g.102978719G>C | GRCh38 |
| NC_000001.10:g.103444275G>C , CM000663.1:g.103444275G>C | GRCh37 |
| NC_000001.9:g.103216863G>C | NCBI36 |
| NG_008033.1:g.134778C>G | |
| NG_008033.2:g.134778C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370096.9:c.2743C>G MANE Select | ENSP00000359114.3:p.Pro915Ala | |
| ENST00000353414.8:c.2626C>G | ENSP00000302551.6:p.Pro876Ala | |
| ENST00000358392.6:c.2779C>G | ENSP00000351163.2:p.Pro927Ala | |
| ENST00000370096.7:c.2743C>G | ENSP00000359114.3:p.Pro915Ala | |
| ENST00000512756.5:c.2395C>G | ENSP00000426533.1:p.Pro799Ala | |
| ENST00000635193.1:c.2077C>G | ||
| NM_001190709.1:c.2626C>G | NP_001177638.1:p.Pro876Ala | |
| NM_001854.3:c.2743C>G | NP_001845.3:p.Pro915Ala | |
| NM_080629.2:c.2779C>G | NP_542196.2:p.Pro927Ala | |
| NM_080630.3:c.2395C>G | NP_542197.3:p.Pro799Ala | |
| XM_011540719.1:c.2743C>G | XP_011539021.1:p.Pro915Ala | |
| XM_011540720.1:c.976C>G | XP_011539022.1:p.Pro326Ala | |
| XM_011540721.1:c.331C>G | XP_011539023.1:p.Pro111Ala | |
| XR_946545.1:n.3157C>G | ||
| NR_134980.1:n.3077C>G | ||
| XM_017000334.1:c.2896C>G | XP_016855823.1:p.Pro966Ala | |
| XM_017000335.1:c.2890C>G | XP_016855824.1:p.Pro964Ala | |
| XM_017000336.1:c.2896C>G | XP_016855825.1:p.Pro966Ala | |
| XM_017000337.1:c.1294C>G | XP_016855826.1:p.Pro432Ala | |
| NM_001854.4:c.2743C>G MANE Select | NP_001845.3:p.Pro915Ala | |
| NM_080630.4:c.2395C>G | NP_542197.3:p.Pro799Ala | |
| NR_134980.2:n.3103C>G | ||
| NM_001190709.2:c.2626C>G | NP_001177638.1:p.Pro876Ala | |
| NM_080629.3:c.2779C>G | NP_542196.2:p.Pro927Ala |