Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.40845268G>A , CM000681.2:g.40845268G>A | GRCh38 |
| NC_000019.9:g.41351173G>A , CM000681.1:g.41351173G>A | GRCh37 |
| NC_000019.8:g.46043013G>A | NCBI36 |
| NG_008377.1:g.10180C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000301141.10:c.1161+26C>T MANE Select | ENSP00000301141.4:n.1161+26C>T | |
| ENST00000301141.9:c.1161+26C>T | ENSP00000301141.4:n.1161+26C>T | |
| ENST00000596719.5:n.1038C>T | ||
| ENST00000601627.1:c.119+43853G>A | ||
| ENST00000610301.1:c.1161+26C>T | ENSP00000477899.1:n.1161+26C>T | |
| NM_000762.5:c.1161+26C>T | NP_000753.3:n.1161+26C>T | |
| NM_000762.6:c.1161+26C>T MANE Select | NP_000753.3:n.1161+26C>T |