Linked Data
gnomAD v4:
22-32474901-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32474901C>A , CM000684.2:g.32474901C>A | GRCh38 |
| NC_000022.10:g.32870888C>A , CM000684.1:g.32870888C>A | GRCh37 |
| NC_000022.9:g.31200888C>A | NCBI36 |
| NG_016001.1:g.5182C>A | |
| NG_016001.2:g.5182C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266087.12:c.-102C>A MANE Select | ENSP00000266087.7:n.-102C>A | |
| ENST00000266087.11:c.-102C>A | ENSP00000266087.7:n.-102C>A | |
| ENST00000420700.5:c.-102C>A | ENSP00000406155.1:n.-102C>A | |
| ENST00000425028.5:c.-102C>A | ENSP00000395823.1:n.-102C>A | |
| NM_012179.3:c.-102C>A | NP_036311.3:n.-102C>A | |
| XM_011530106.1:c.-275C>A | XP_011528408.1:n.-275C>A | |
| XM_024452207.1:c.-292C>A | XP_024307975.1:n.-292C>A | |
| NM_012179.4:c.-102C>A MANE Select | NP_036311.3:n.-102C>A |