Linked Data
ClinVar Variation Id:
923802
dbSNP Id:
rs543615478
ExAC:
7:150644448 G / A
gnomAD v2:
7-150644448-G-A
gnomAD v3:
7-150947360-G-A
gnomAD v4:
7-150947360-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150947360G>A , CM000669.2:g.150947360G>A | GRCh38 |
| NC_000007.13:g.150644448G>A , CM000669.1:g.150644448G>A | GRCh37 |
| NC_000007.12:g.150275381G>A | NCBI36 |
| NG_008916.1:g.35567C>T , LRG_288:g.35567C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684241.1:n.3953C>T | ||
| ENST00000262186.10:c.3120C>T MANE Select | ENSP00000262186.5:p.Ser1040= | |
| ENST00000330883.9:c.2100C>T | ENSP00000328531.4:p.Ser700= | |
| ENST00000262186.9:c.3120C>T | ENSP00000262186.5:p.Ser1040= | |
| ENST00000330883.8:c.2100C>T | ENSP00000328531.4:p.Ser700= | |
| NM_000238.3:c.3120C>T , LRG_288t1:c.3120C>T | NP_000229.1:p.Ser1040= | |
| NM_172057.2:c.2100C>T , LRG_288t3:c.2100C>T | NP_742054.1:p.Ser700= | |
| XM_011516185.1:c.2820C>T | XP_011514487.1:p.Ser940= | |
| XM_011516185.2:c.2820C>T | XP_011514487.1:p.Ser940= | |
| XM_017012195.1:c.2970C>T | XP_016867684.1:p.Ser990= | |
| XM_017012196.1:c.2943C>T | XP_016867685.1:p.Ser981= | |
| NM_000238.4:c.3120C>T MANE Select | NP_000229.1:p.Ser1040= | |
| NM_172057.3:c.2100C>T | NP_742054.1:p.Ser700= |