Linked Data
ClinVar Variation Id:
834430
ClinVar RCV Id:
RCV001035113
dbSNP Id:
rs1801441796
gnomAD v4:
7-150958146-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150958146C>A , CM000669.2:g.150958146C>A | GRCh38 |
| NC_000007.13:g.150655234C>A , CM000669.1:g.150655234C>A | GRCh37 |
| NC_000007.12:g.150286167C>A | NCBI36 |
| NG_008916.1:g.24781G>T , LRG_288:g.24781G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684241.1:n.1662G>T | ||
| ENST00000262186.10:c.829G>T MANE Select | ENSP00000262186.5:p.Ala277Ser | |
| ENST00000262186.9:c.829G>T | ENSP00000262186.5:p.Ala277Ser | |
| ENST00000430723.4:c.481G>T | ENSP00000387657.4:p.Ala161Ser | |
| ENST00000532957.5:n.1052G>T | ||
| NM_000238.3:c.829G>T , LRG_288t1:c.829G>T | NP_000229.1:p.Ala277Ser | |
| NM_172056.2:c.829G>T , LRG_288t2:c.829G>T | NP_742053.1:p.Ala277Ser | |
| XM_011516185.1:c.529G>T | XP_011514487.1:p.Ala177Ser | |
| XM_011516186.1:c.829G>T | XP_011514488.1:p.Ala277Ser | |
| XM_011516185.2:c.529G>T | XP_011514487.1:p.Ala177Ser | |
| XM_011516186.3:c.829G>T | XP_011514488.1:p.Ala277Ser | |
| XM_017012195.1:c.679G>T | XP_016867684.1:p.Ala227Ser | |
| XM_017012196.1:c.652G>T | XP_016867685.1:p.Ala218Ser | |
| NM_000238.4:c.829G>T MANE Select | NP_000229.1:p.Ala277Ser |