Linked Data
gnomAD v4:
3-190405007-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190405007C>A , CM000665.2:g.190405007C>A | GRCh38 |
| NC_000003.11:g.190122796C>A , CM000665.1:g.190122796C>A | GRCh37 |
| NC_000003.10:g.191605490C>A | NCBI36 |
| NG_008149.1:g.21956C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264734.3:c.382+81C>A MANE Select | ENSP00000264734.3:n.382+81C>A | |
| ENST00000456423.2:c.115-4896C>A | ENSP00000414136.2:n.115-4896C>A | |
| ENST00000264734.2:c.592+81C>A | ENSP00000264734.2:n.592+81C>A | |
| ENST00000456423.1:c.325-4896C>A | ENSP00000414136.1:n.325-4896C>A | |
| NM_006580.3:c.592+81C>A | NP_006571.1:n.592+81C>A | |
| NM_001378492.1:c.382+81C>A | NP_001365421.1:n.382+81C>A | |
| NM_001378493.1:c.382+81C>A | NP_001365422.1:n.382+81C>A | |
| NM_006580.4:c.382+81C>A MANE Select | NP_006571.2:n.382+81C>A |