Linked Data
gnomAD v4:
9-97853886-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.97853886A>G , CM000671.2:g.97853886A>G | GRCh38 |
| NC_000009.11:g.100616168A>G , CM000671.1:g.100616168A>G | GRCh37 |
| NC_000009.10:g.99655989A>G | NCBI36 |
| NG_011979.1:g.5632A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375123.5:c.-29A>G MANE Select | ENSP00000364265.3:n.-29A>G | |
| ENST00000375123.4:c.-29A>G | ENSP00000364265.3:n.-29A>G | |
| NM_004473.3:c.-29A>G | NP_004464.2:n.-29A>G | |
| NM_004473.4:c.-29A>G MANE Select | NP_004464.2:n.-29A>G |