Linked Data
gnomAD v4:
22-32049797-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32049797T>C , CM000684.2:g.32049797T>C | GRCh38 |
| NC_000022.10:g.32445784T>C , CM000684.1:g.32445784T>C | GRCh37 |
| NC_000022.9:g.30775784T>C | NCBI36 |
| NG_017045.1:g.11766T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266088.9:c.136-146T>C MANE Select | ENSP00000266088.4:n.136-146T>C | |
| ENST00000266088.8:c.136-146T>C | ENSP00000266088.4:n.136-146T>C | |
| NM_000343.3:c.136-146T>C | NP_000334.1:n.136-146T>C | |
| XM_011530331.1:c.136-146T>C | XP_011528633.1:n.136-146T>C | |
| NM_000343.4:c.136-146T>C MANE Select | NP_000334.1:n.136-146T>C |