Linked Data
ClinVar Variation Id:
67533
dbSNP Id:
rs199472878
gnomAD v3:
7-150958145-G-T
gnomAD v4:
7-150958145-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150958145G>T , CM000669.2:g.150958145G>T | GRCh38 |
| NC_000007.13:g.150655233G>T , CM000669.1:g.150655233G>T | GRCh37 |
| NC_000007.12:g.150286166G>T | NCBI36 |
| NG_008916.1:g.24782C>A , LRG_288:g.24782C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000684241.1:n.1663C>A | ||
| ENST00000262186.10:c.830C>A MANE Select | ENSP00000262186.5:p.Ala277Asp | |
| ENST00000262186.9:c.830C>A | ENSP00000262186.5:p.Ala277Asp | |
| ENST00000430723.4:c.482C>A | ENSP00000387657.4:p.Ala161Asp | |
| ENST00000532957.5:n.1053C>A | ||
| NM_000238.3:c.830C>A , LRG_288t1:c.830C>A | NP_000229.1:p.Ala277Asp | |
| NM_172056.2:c.830C>A , LRG_288t2:c.830C>A | NP_742053.1:p.Ala277Asp | |
| XM_011516185.1:c.530C>A | XP_011514487.1:p.Ala177Asp | |
| XM_011516186.1:c.830C>A | XP_011514488.1:p.Ala277Asp | |
| XM_011516185.2:c.530C>A | XP_011514487.1:p.Ala177Asp | |
| XM_011516186.3:c.830C>A | XP_011514488.1:p.Ala277Asp | |
| XM_017012195.1:c.680C>A | XP_016867684.1:p.Ala227Asp | |
| XM_017012196.1:c.653C>A | XP_016867685.1:p.Ala218Asp | |
| NM_000238.4:c.830C>A MANE Select | NP_000229.1:p.Ala277Asp |