Linked Data
ClinVar Variation Id:
536388
dbSNP Id:
rs368269464
ExAC:
9:135140000 A / T
gnomAD v2:
9-135140000-A-T
gnomAD v3:
9-132264613-A-T
gnomAD v4:
9-132264613-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.132264613A>T , CM000671.2:g.132264613A>T | GRCh38 |
| NC_000009.11:g.135140000A>T , CM000671.1:g.135140000A>T | GRCh37 |
| NC_000009.10:g.134129821A>T | NCBI36 |
| NG_007946.1:g.95373T>A , LRG_268:g.95373T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000224140.6:c.7660T>A MANE Select | ENSP00000224140.5:p.Phe2554Ile | |
| ENST00000224140.5:c.7660T>A | ENSP00000224140.5:p.Phe2554Ile | |
| ENST00000436441.5:c.2473T>A | ENSP00000409143.1:p.Phe825Ile | |
| ENST00000477049.1:n.810T>A | ||
| NM_015046.5:c.7660T>A , LRG_268t1:c.7660T>A | NP_055861.3:p.Phe2554Ile | |
| XM_005272171.1:c.7747T>A | XP_005272228.1:p.Phe2583Ile | |
| XM_005272172.1:c.7747T>A | XP_005272229.1:p.Phe2583Ile | |
| XM_005272173.1:c.7747T>A | XP_005272230.1:p.Phe2583Ile | |
| XM_011518404.1:c.7747T>A | XP_011516706.1:p.Phe2583Ile | |
| XM_011518405.1:c.7747T>A | XP_011516707.1:p.Phe2583Ile | |
| XR_929739.1:n.7576T>A | ||
| NM_001351527.1:c.7660T>A | NP_001338456.1:p.Phe2554Ile | |
| NM_001351528.1:c.7747T>A | NP_001338457.1:p.Phe2583Ile | |
| NM_015046.6:c.7660T>A | NP_055861.3:p.Phe2554Ile | |
| XM_005272172.3:c.7747T>A | XP_005272229.1:p.Phe2583Ile | |
| XM_005272173.3:c.7747T>A | XP_005272230.1:p.Phe2583Ile | |
| XM_011518404.3:c.7747T>A | XP_011516706.1:p.Phe2583Ile | |
| XM_011518405.3:c.7747T>A | XP_011516707.1:p.Phe2583Ile | |
| XM_017014496.1:c.2200T>A | XP_016869985.1:p.Phe734Ile | |
| XR_001746251.1:n.7215T>A | ||
| XR_929739.2:n.7576T>A | ||
| NM_015046.7:c.7660T>A MANE Select | NP_055861.3:p.Phe2554Ile | |
| NM_001351528.2:c.7747T>A | NP_001338457.1:p.Phe2583Ile | |
| NM_001351527.2:c.7660T>A | NP_001338456.1:p.Phe2554Ile |