Linked Data
dbSNP Id:
rs561123236
gnomAD v2:
9-33122627-G-A
gnomAD v3:
9-33122629-G-A
gnomAD v4:
9-33122629-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.33122629G>A , CM000671.2:g.33122629G>A | GRCh38 |
| NC_000009.11:g.33122627G>A , CM000671.1:g.33122627G>A | GRCh37 |
| NC_000009.10:g.33112627G>A | NCBI36 |
| NG_008919.1:g.49730C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379731.5:c.649-2023C>T MANE Select | ENSP00000369055.4:n.649-2023C>T | |
| ENST00000379731.4:c.649-2023C>T | ENSP00000369055.4:n.649-2023C>T | |
| ENST00000535206.5:c.648+12560C>T | ENSP00000440341.1:n.648+12560C>T | |
| NM_001497.3:c.649-2023C>T | NP_001488.2:n.649-2023C>T | |
| XM_005251440.3:c.649-2023C>T | XP_005251497.1:n.649-2023C>T | |
| XM_005251440.5:c.649-2023C>T | XP_005251497.1:n.649-2023C>T | |
| NM_001378495.1:c.610-2023C>T | NP_001365424.1:n.610-2023C>T | |
| NM_001378496.1:c.649-2023C>T | NP_001365425.1:n.649-2023C>T | |
| NM_001378497.1:c.648+12560C>T | NP_001365426.1:n.648+12560C>T | |
| NM_001497.4:c.649-2023C>T MANE Select | NP_001488.2:n.649-2023C>T |