Linked Data
gnomAD v4:
17-8085929-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8085929G>T , CM000679.2:g.8085929G>T | GRCh38 |
| NC_000017.10:g.7989247G>T , CM000679.1:g.7989247G>T | GRCh37 |
| NC_000017.9:g.7929972G>T | NCBI36 |
| NG_007099.1:g.6775C>A | |
| NG_007099.2:g.6788C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647874.1:c.352+87C>A MANE Select | ENSP00000497784.1:n.352+87C>A | |
| ENST00000319144.4:c.352+87C>A | ENSP00000315167.4:n.352+87C>A | |
| NM_001139.2:c.352+87C>A | NP_001130.1:n.352+87C>A | |
| NM_001139.3:c.352+87C>A MANE Select | NP_001130.1:n.352+87C>A |