Linked Data
gnomAD v4:
16-67436437-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67436437T>G , CM000678.2:g.67436437T>G | GRCh38 |
| NC_000016.9:g.67470340T>G , CM000678.1:g.67470340T>G | GRCh37 |
| NC_000016.8:g.66027841T>G | NCBI36 |
| NG_011482.1:g.49750A>C | |
| NG_016549.1:g.10305T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326152.6:c.802+51T>G MANE Select | ENSP00000316786.5:n.802+51T>G | |
| ENST00000326152.5:c.802+51T>G | ENSP00000316786.5:n.802+51T>G | |
| NM_000196.3:c.802+51T>G | NP_000187.3:n.802+51T>G | |
| NM_000196.4:c.802+51T>G MANE Select | NP_000187.3:n.802+51T>G |