Linked Data
ClinVar Variation Id:
456939
dbSNP Id:
rs1361757645
gnomAD v2:
7-150655328-G-T
gnomAD v3:
7-150958240-G-T
gnomAD v4:
7-150958240-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150958240G>T , CM000669.2:g.150958240G>T | GRCh38 |
| NC_000007.13:g.150655328G>T , CM000669.1:g.150655328G>T | GRCh37 |
| NC_000007.12:g.150286261G>T | NCBI36 |
| NG_008916.1:g.24687C>A , LRG_288:g.24687C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684241.1:n.1568C>A | ||
| ENST00000262186.10:c.735C>A MANE Select | ENSP00000262186.5:p.Pro245= | |
| ENST00000262186.9:c.735C>A | ENSP00000262186.5:p.Pro245= | |
| ENST00000430723.4:c.387C>A | ENSP00000387657.4:p.Pro129= | |
| ENST00000532957.5:n.958C>A | ||
| NM_000238.3:c.735C>A , LRG_288t1:c.735C>A | NP_000229.1:p.Pro245= | |
| NM_172056.2:c.735C>A , LRG_288t2:c.735C>A | NP_742053.1:p.Pro245= | |
| XM_011516185.1:c.435C>A | XP_011514487.1:p.Pro145= | |
| XM_011516186.1:c.735C>A | XP_011514488.1:p.Pro245= | |
| XM_011516185.2:c.435C>A | XP_011514487.1:p.Pro145= | |
| XM_011516186.3:c.735C>A | XP_011514488.1:p.Pro245= | |
| XM_017012195.1:c.585C>A | XP_016867684.1:p.Pro195= | |
| XM_017012196.1:c.558C>A | XP_016867685.1:p.Pro186= | |
| NM_000238.4:c.735C>A MANE Select | NP_000229.1:p.Pro245= |