Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15180765C>G , CM000681.2:g.15180765C>G | GRCh38 |
| NC_000019.9:g.15291576C>G , CM000681.1:g.15291576C>G | GRCh37 |
| NC_000019.8:g.15152576C>G | NCBI36 |
| NG_009819.1:g.25217G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000435.3:c.3058G>C MANE Select | NP_000426.2:p.Ala1020Pro |
| ENST00000263388.7:c.3058G>C MANE Select | ENSP00000263388.1:p.Ala1020Pro |
| NM_000435.2:c.3058G>C | NP_000426.2:p.Ala1020Pro |
| ENST00000263388.6:c.3058G>C | ENSP00000263388.1:p.Ala1020Pro |
| ENST00000601011.1:c.2899G>C | ENSP00000473138.1:p.Ala967Pro |
| XM_005259924.3:c.2902G>C | XP_005259981.1:p.Ala968Pro |
| XM_005259924.4:c.2902G>C | XP_005259981.1:p.Ala968Pro |