Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18787441C>A , CM000681.2:g.18787441C>A | GRCh38 |
| NC_000019.9:g.18898250C>A , CM000681.1:g.18898250C>A | GRCh37 |
| NC_000019.8:g.18759250C>A | NCBI36 |
| NG_007070.1:g.8865G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.1135+50G>T MANE Select | ENSP00000222271.2:n.1135+50G>T | |
| ENST00000222271.6:c.1135+50G>T | ENSP00000222271.2:n.1135+50G>T | |
| ENST00000425807.1:c.976+50G>T | ENSP00000403792.1:n.976+50G>T | |
| ENST00000542601.6:c.1036+50G>T | ENSP00000439156.2:n.1036+50G>T | |
| NM_000095.2:c.1135+50G>T | NP_000086.2:n.1135+50G>T | |
| NM_000095.3:c.1135+50G>T MANE Select | NP_000086.2:n.1135+50G>T |