Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.101428594A= , CM000671.2:g.101428594A= | GRCh38 |
| NC_000009.11:g.104190876A= , CM000671.1:g.104190876A= | GRCh37 |
| NC_000009.10:g.103230697A= | NCBI36 |
| NG_012387.1:g.12187T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647789.2:c.325-71T= MANE Select | ENSP00000497767.1:n.325-71T= | |
| ENST00000648064.1:c.325-71T= | ENSP00000497990.1:n.325-71T= | |
| ENST00000648758.1:c.325-71T= | ENSP00000497731.1:n.325-71T= | |
| ENST00000649902.1:c.325-71T= | ENSP00000497216.1:n.325-71T= | |
| ENST00000374855.8:c.325-71T= | ENSP00000363988.4:n.325-71T= | |
| ENST00000468981.3:n.67+1215T= | ||
| ENST00000616752.1:c.325-71T= | ENSP00000481363.1:n.325-71T= | |
| NM_000035.3:c.325-71T= | NP_000026.2:n.325-71T= | |
| NM_000035.4:c.325-71T= MANE Select | NP_000026.2:n.325-71T= |