Linked Data
MyVariant Identifiers:
chr9:g.32550856T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.32550858T>A , CM000671.2:g.32550858T>A | GRCh38 |
| NC_000009.11:g.32550856T>A , CM000671.1:g.32550856T>A | GRCh37 |
| NC_000009.10:g.32540856T>A | NCBI36 |
| NG_017050.1:g.6767A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360538.7:c.114A>T MANE Select | ENSP00000353735.2:p.Gly38= | |
| ENST00000680198.1:c.114A>T | ENSP00000505143.1:p.Gly38= | |
| ENST00000681750.1:c.-129A>T | ENSP00000506413.1:n.-129A>T | |
| ENST00000360538.6:c.114A>T | ENSP00000353735.2:p.Gly38= | |
| ENST00000379858.1:c.3+1576A>T | ENSP00000369187.1:n.3+1576A>T | |
| NM_001195622.1:c.3+1576A>T | NP_001182551.1:n.3+1576A>T | |
| NM_005802.4:c.114A>T | NP_005793.2:p.Gly38= | |
| NM_005802.5:c.114A>T MANE Select | NP_005793.2:p.Gly38= | |
| NM_001195622.2:c.3+1576A>T | NP_001182551.1:n.3+1576A>T |