Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8073764G>T , CM000679.2:g.8073764G>T | GRCh38 |
| NC_000017.10:g.7977082G>T , CM000679.1:g.7977082G>T | GRCh37 |
| NC_000017.9:g.7917807G>T | NCBI36 |
| NG_007099.1:g.18940C>A | |
| NG_007099.2:g.18953C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001139.3:c.1655-7C>A MANE Select | NP_001130.1:n.1655-7C>A |
| ENST00000647874.1:c.1655-7C>A MANE Select | ENSP00000497784.1:n.1655-7C>A |
| NM_001139.2:c.1655-7C>A | NP_001130.1:n.1655-7C>A |
| ENST00000319144.4:c.1655-7C>A | ENSP00000315167.4:n.1655-7C>A |
| ENST00000577351.5:n.480-446C>A | |
| ENST00000649809.1:c.719-7C>A | ENSP00000496845.1:n.719-7C>A |
| ENST00000650441.1:n.78-7C>A |