Linked Data
dbSNP Id:
rs770628368
ExAC:
9:32550773 T / A
gnomAD v2:
9-32550773-T-A
gnomAD v4:
9-32550775-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.32550775T>A , CM000671.2:g.32550775T>A | GRCh38 |
| NC_000009.11:g.32550773T>A , CM000671.1:g.32550773T>A | GRCh37 |
| NC_000009.10:g.32540773T>A | NCBI36 |
| NG_017050.1:g.6850A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360538.7:c.197A>T MANE Select | ENSP00000353735.2:p.Glu66Val | |
| ENST00000680198.1:c.197A>T | ENSP00000505143.1:p.Glu66Val | |
| ENST00000681750.1:c.-46A>T | ENSP00000506413.1:n.-46A>T | |
| ENST00000360538.6:c.197A>T | ENSP00000353735.2:p.Glu66Val | |
| ENST00000379858.1:c.3+1659A>T | ENSP00000369187.1:n.3+1659A>T | |
| NM_001195622.1:c.3+1659A>T | NP_001182551.1:n.3+1659A>T | |
| NM_005802.4:c.197A>T | NP_005793.2:p.Glu66Val | |
| NM_005802.5:c.197A>T MANE Select | NP_005793.2:p.Glu66Val | |
| NM_001195622.2:c.3+1659A>T | NP_001182551.1:n.3+1659A>T |