Linked Data
gnomAD v4:
1-17027561-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17027561C>A , CM000663.2:g.17027561C>A | GRCh38 |
| NC_000001.10:g.17354056C>A , CM000663.1:g.17354056C>A | GRCh37 |
| NC_000001.9:g.17226643C>A | NCBI36 |
| NG_012340.1:g.31610G>T , LRG_316:g.31610G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463045.3:c.369+188G>T | ENSP00000481376.2:n.369+188G>T | |
| ENST00000491274.6:c.498+188G>T | ENSP00000480482.2:n.498+188G>T | |
| ENST00000375499.8:c.540+188G>T MANE Select | ENSP00000364649.3:n.540+188G>T | |
| ENST00000375499.7:c.540+188G>T | ENSP00000364649.3:n.540+188G>T | |
| ENST00000485515.5:n.474+188G>T | ||
| ENST00000491274.5:c.498+188G>T | ENSP00000480482.1:n.498+188G>T | |
| NM_003000.2:c.540+188G>T , LRG_316t1:c.540+188G>T | NP_002991.2:n.540+188G>T | |
| NM_003000.3:c.540+188G>T MANE Select | NP_002991.2:n.540+188G>T |