Linked Data
gnomAD v4:
12-5043936-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5043936A>G , CM000674.2:g.5043936A>G | GRCh38 |
| NC_000012.11:g.5153102A>G , CM000674.1:g.5153102A>G | GRCh37 |
| NC_000012.10:g.5023363A>G | NCBI36 |
| NG_012198.1:g.5018A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.-212A>G MANE Select | ENSP00000252321.3:n.-212A>G | |
| NM_002234.3:c.-212A>G | NP_002225.2:n.-212A>G | |
| NM_002234.4:c.-212A>G MANE Select | NP_002225.2:n.-212A>G |