Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.149570207A>C , CM000664.2:g.149570207A>C | GRCh38 |
| NC_000002.11:g.150426721A>C , CM000664.1:g.150426721A>C | GRCh37 |
| NC_000002.10:g.150134967A>C | NCBI36 |
| NG_009189.1:g.22610T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303319.10:c.697-39T>G MANE Select | ENSP00000301920.5:n.697-39T>G | |
| ENST00000303319.9:c.697-39T>G | ENSP00000301920.5:n.697-39T>G | |
| ENST00000422782.2:c.799-39T>G | ENSP00000408331.2:n.799-39T>G | |
| ENST00000428879.5:c.697-39T>G | ENSP00000389060.1:n.697-39T>G | |
| NM_015702.2:c.697-39T>G | NP_056517.1:n.697-39T>G | |
| NM_015702.3:c.697-39T>G MANE Select | NP_056517.1:n.697-39T>G |