Linked Data
gnomAD v4:
6-131890332-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.131890332T>G , CM000668.2:g.131890332T>G | GRCh38 |
| NC_000006.11:g.132211472T>G , CM000668.1:g.132211472T>G | GRCh37 |
| NC_000006.10:g.132253165T>G | NCBI36 |
| NG_008206.1:g.87317T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684674.1:n.1039-9T>G | ||
| ENST00000647893.1:c.2608-9T>G MANE Select | ENSP00000498074.1:n.2608-9T>G | |
| ENST00000360971.6:c.2608-9T>G | ENSP00000354238.2:n.2608-9T>G | |
| ENST00000513998.5:c.*1445-9T>G | ENSP00000422424.1:n.*1445-9T>G | |
| NM_006208.2:c.2608-9T>G | NP_006199.2:n.2608-9T>G | |
| XM_011535896.1:c.1498-9T>G | XP_011534198.1:n.1498-9T>G | |
| NM_006208.3:c.2608-9T>G MANE Select | NP_006199.2:n.2608-9T>G |