Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.110913225T>G , CM000674.2:g.110913225T>G | GRCh38 |
| NC_000012.11:g.111351029T>G , CM000674.1:g.111351029T>G | GRCh37 |
| NC_000012.10:g.109835412T>G | NCBI36 |
| NG_007554.1:g.12353A>C , LRG_393:g.12353A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000228841.15:c.353+21A>C MANE Select | ENSP00000228841.8:n.353+21A>C | |
| ENST00000663220.1:c.296+21A>C | ENSP00000499568.1:n.296+21A>C | |
| ENST00000228841.12:c.353+21A>C | ENSP00000228841.7:n.353+21A>C | |
| ENST00000548438.1:c.311+21A>C | ENSP00000447154.1:n.311+21A>C | |
| ENST00000549029.1:n.205A>C | ||
| NM_000432.3:c.353+21A>C , LRG_393t1:c.353+21A>C | NP_000423.2:n.353+21A>C | |
| NM_000432.4:c.353+21A>C MANE Select | NP_000423.2:n.353+21A>C |