Linked Data
gnomAD v4:
17-40866617-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.40866617T>G , CM000679.2:g.40866617T>G | GRCh38 |
| NC_000017.10:g.39022869T>G , CM000679.1:g.39022869T>G | GRCh37 |
| NC_000017.9:g.36276395T>G | NCBI36 |
| NG_008077.1:g.5594A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251643.5:c.567+3A>C MANE Select | ENSP00000251643.4:n.567+3A>C | |
| ENST00000647902.1:c.459+3A>C | ENSP00000497770.1:n.459+3A>C | |
| ENST00000251643.4:c.567+3A>C | ENSP00000251643.4:n.567+3A>C | |
| NM_000223.3:c.567+3A>C | NP_000214.1:n.567+3A>C | |
| XR_934754.1:n.1500+15757T>G | ||
| XR_934754.2:n.2008+15757T>G | ||
| NM_000223.4:c.567+3A>C MANE Select | NP_000214.1:n.567+3A>C |