Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94427062G>A , CM000669.2:g.94427062G>A | GRCh38 |
| NC_000007.13:g.94056374G>A , CM000669.1:g.94056374G>A | GRCh37 |
| NC_000007.12:g.93894310G>A | NCBI36 |
| NG_007405.1:g.37502G>A , LRG_2:g.37502G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.3159+1G>A MANE Select | NP_000080.2:n.3159+1G>A |
| ENST00000297268.11:c.3159+1G>A MANE Select | ENSP00000297268.6:n.3159+1G>A |
| NM_000089.3:c.3159+1G>A , LRG_2t1:c.3159+1G>A | NP_000080.2:n.3159+1G>A |
| ENST00000297268.10:c.3159+1G>A | ENSP00000297268.6:n.3159+1G>A |
| ENST00000481570.5:n.3609+1G>A | |
| ENST00000488121.1:n.75+1G>A | |
| ENST00000492110.1:n.279+1G>A | |
| ENST00000620463.1:c.3153+1G>A | ENSP00000477719.1:n.3153+1G>A |