Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.66228153C>T , CM000679.2:g.66228153C>T | GRCh38 |
| NC_000017.10:g.64224271C>T , CM000679.1:g.64224271C>T | GRCh37 |
| NC_000017.9:g.61654733C>T | NCBI36 |
| NG_012045.1:g.6286G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000042.3:c.108G>A MANE Select | NP_000033.2:p.Pro36= |
| ENST00000205948.11:c.108G>A MANE Select | ENSP00000205948.6:p.Pro36= |
| NM_000042.2:c.108G>A | NP_000033.2:p.Pro36= |
| ENST00000205948.10:c.108G>A | ENSP00000205948.6:p.Pro36= |
| ENST00000577982.1:c.108G>A | ENSP00000464301.1:p.Pro36= |
| ENST00000581797.5:c.-73G>A | ENSP00000463553.1:n.-73G>A |