Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17024076T>C , CM000663.2:g.17024076T>C | GRCh38 |
| NC_000001.10:g.17350571T>C , CM000663.1:g.17350571T>C | GRCh37 |
| NC_000001.9:g.17223158T>C | NCBI36 |
| NG_012340.1:g.35095A>G , LRG_316:g.35095A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000463045.3:c.370-2A>G | ENSP00000481376.2:n.370-2A>G | |
| ENST00000491274.6:c.499-2A>G | ENSP00000480482.2:n.499-2A>G | |
| ENST00000375499.8:c.541-2A>G MANE Select | ENSP00000364649.3:n.541-2A>G | |
| ENST00000375499.7:c.541-2A>G | ENSP00000364649.3:n.541-2A>G | |
| ENST00000485515.5:n.475-2A>G | ||
| ENST00000491274.5:c.499-2A>G | ENSP00000480482.1:n.499-2A>G | |
| NM_003000.2:c.541-2A>G , LRG_316t1:c.541-2A>G | NP_002991.2:n.541-2A>G | |
| NM_003000.3:c.541-2A>G MANE Select | NP_002991.2:n.541-2A>G |