Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.14977895G>A , CM000674.2:g.14977895G>A | GRCh38 |
| NC_000012.11:g.15130829G>A , CM000674.1:g.15130829G>A | GRCh37 |
| NC_000012.10:g.15022096G>A | NCBI36 |
| NG_016859.1:g.9874G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266395.3:c.-41-77G>A MANE Select | ENSP00000266395.2:n.-41-77G>A | |
| ENST00000266395.2:c.-41-77G>A | ENSP00000266395.2:n.-41-77G>A | |
| NM_006205.2:c.-41-77G>A | NP_006196.1:n.-41-77G>A | |
| XR_931376.1:n.175+11592C>T | ||
| XM_017019431.2:c.-118G>A | XP_016874920.1:n.-118G>A | |
| XR_931376.2:n.389+11592C>T | ||
| NM_006205.3:c.-41-77G>A MANE Select | NP_006196.1:n.-41-77G>A |