Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.176117597G>A , CM000664.2:g.176117597G>A | GRCh38 |
| NC_000002.11:g.176982325G>A , CM000664.1:g.176982325G>A | GRCh37 |
| NC_000002.10:g.176690571G>A | NCBI36 |
| NG_008133.2:g.10834G>A , LRG_246:g.10834G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249501.5:c.745+19G>A MANE Select | ENSP00000249501.4:n.745+19G>A | |
| ENST00000249501.4:c.745+19G>A | ENSP00000249501.4:n.745+19G>A | |
| ENST00000490088.2:n.570-1357G>A | ||
| ENST00000549469.1:n.617-1357G>A | ||
| NM_002148.3:c.745+19G>A , LRG_246t1:c.745+19G>A | NP_002139.2:n.745+19G>A | |
| NM_002148.4:c.745+19G>A MANE Select | NP_002139.2:n.745+19G>A |