Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136687154T>A , CM000671.2:g.136687154T>A | GRCh38 |
| NC_000009.11:g.139581606T>A , CM000671.1:g.139581606T>A | GRCh37 |
| NC_000009.10:g.138701427T>A | NCBI36 |
| NG_008090.1:g.5306A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371696.7:c.182+22A>T MANE Select | ENSP00000360761.2:n.182+22A>T | |
| ENST00000371694.7:c.182+22A>T | ENSP00000360759.3:n.182+22A>T | |
| ENST00000371696.6:c.182+22A>T | ENSP00000360761.2:n.182+22A>T | |
| ENST00000470861.1:n.190+22A>T | ||
| ENST00000538402.1:c.182+22A>T | ENSP00000438919.1:n.182+22A>T | |
| NM_001012727.1:c.182+22A>T | NP_001012745.1:n.182+22A>T | |
| NM_006412.3:c.182+22A>T | NP_006403.2:n.182+22A>T | |
| NM_006412.4:c.182+22A>T MANE Select | NP_006403.2:n.182+22A>T | |
| NM_001012727.2:c.182+22A>T | NP_001012745.1:n.182+22A>T |