Linked Data
gnomAD v4:
13-110179152-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110179152A>C , CM000675.2:g.110179152A>C | GRCh38 |
| NC_000013.10:g.110831499A>C , CM000675.1:g.110831499A>C | GRCh37 |
| NC_000013.9:g.109629500A>C | NCBI36 |
| NG_011544.2:g.132998T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375820.10:c.2345-116T>G MANE Select | ENSP00000364979.4:n.2345-116T>G | |
| ENST00000649738.1:n.2475-116T>G | ||
| ENST00000375820.8:c.2345-116T>G | ENSP00000364979.4:n.2345-116T>G | |
| NM_001845.5:c.2345-116T>G | NP_001836.3:n.2345-116T>G | |
| XM_011521048.1:c.2153-116T>G | XP_011519350.1:n.2153-116T>G | |
| XM_011521048.2:c.2153-116T>G | XP_011519350.1:n.2153-116T>G | |
| NM_001845.6:c.2345-116T>G MANE Select | NP_001836.3:n.2345-116T>G |