Linked Data
gnomAD v4:
16-67436557-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67436557T>A , CM000678.2:g.67436557T>A | GRCh38 |
| NC_000016.9:g.67470460T>A , CM000678.1:g.67470460T>A | GRCh37 |
| NC_000016.8:g.66027961T>A | NCBI36 |
| NG_011482.1:g.49630A>T | |
| NG_016549.1:g.10425T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326152.6:c.803-31T>A MANE Select | ENSP00000316786.5:n.803-31T>A | |
| ENST00000326152.5:c.803-31T>A | ENSP00000316786.5:n.803-31T>A | |
| NM_000196.3:c.803-31T>A | NP_000187.3:n.803-31T>A | |
| NM_000196.4:c.803-31T>A MANE Select | NP_000187.3:n.803-31T>A |