Linked Data
dbSNP Id:
rs1832238266
gnomAD v3:
9-128323053-G-T
gnomAD v4:
9-128323053-G-T
MyVariant Identifiers:
chr9:g.131085332G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.128323053G>T , CM000671.2:g.128323053G>T | GRCh38 |
| NC_000009.11:g.131085332G>T , CM000671.1:g.131085332G>T | GRCh37 |
| NC_000009.10:g.130125153G>T | NCBI36 |
| NG_042101.1:g.5546G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300452.8:c.108G>T MANE Select | ENSP00000300452.3:p.Pro36= | |
| ENST00000300452.7:c.108G>T | ENSP00000300452.3:p.Pro36= | |
| ENST00000372875.3:c.108G>T | ENSP00000361966.3:p.Pro36= | |
| ENST00000608951.5:c.108G>T | ENSP00000476323.1:p.Pro36= | |
| ENST00000609948.1:c.108G>T | ENSP00000477292.1:p.Pro36= | |
| NM_001305942.1:c.108G>T | NP_001292871.1:p.Pro36= | |
| NM_016035.3:c.108G>T | NP_057119.2:p.Pro36= | |
| NM_016035.4:c.108G>T | NP_057119.2:p.Pro36= | |
| XM_011518761.1:c.108G>T | XP_011517063.1:p.Pro36= | |
| XR_929805.1:n.454G>T | ||
| XM_017014792.1:c.108G>T | XP_016870281.1:p.Pro36= | |
| XM_017014793.1:c.108G>T | XP_016870282.1:p.Pro36= | |
| XR_001746316.2:n.458G>T | ||
| XR_929805.3:n.454G>T | ||
| NM_016035.5:c.108G>T MANE Select | NP_057119.3:p.Pro36= | |
| NM_001305942.2:c.108G>T | NP_001292871.2:p.Pro36= |