Linked Data
gnomAD v4:
13-33055429-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.33055429C>A , CM000675.2:g.33055429C>A | GRCh38 |
| NC_000013.10:g.33629566C>A , CM000675.1:g.33629566C>A | GRCh37 |
| NC_000013.9:g.32527566C>A | NCBI36 |
| NG_011485.1:g.43996C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380099.4:c.1599+114C>A MANE Select | ENSP00000369442.3:n.1599+114C>A | |
| ENST00000380099.3:c.1599+114C>A | ENSP00000369442.3:n.1599+114C>A | |
| ENST00000487852.1:n.1657+64C>A | ||
| NM_004795.3:c.1599+114C>A | NP_004786.2:n.1599+114C>A | |
| XM_006719895.1:c.678+114C>A | XP_006719958.1:n.678+114C>A | |
| XM_006719895.2:c.678+114C>A | XP_006719958.1:n.678+114C>A | |
| NM_004795.4:c.1599+114C>A MANE Select | NP_004786.2:n.1599+114C>A |