Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.28843051T>C , CM000678.2:g.28843051T>C | GRCh38 |
| NC_000016.9:g.28854372T>C , CM000678.1:g.28854372T>C | GRCh37 |
| NC_000016.8:g.28761873T>C | NCBI36 |
| NG_008964.1:g.8358A>G | |
| NG_029706.2:g.1452T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003321.5:c.1292A>G MANE Select | NP_003312.3:p.Asn431Ser |
| ENST00000313511.8:c.1292A>G MANE Select | ENSP00000322439.3:p.Asn431Ser |
| NM_001365360.1:c.1208A>G | NP_001352289.1:p.Asn403Ser |
| NM_001365360.2:c.1208A>G | NP_001352289.1:p.Asn403Ser |
| NM_003321.4:c.1292A>G | NP_003312.3:p.Asn431Ser |
| ENST00000313511.7:c.1292A>G | ENSP00000322439.3:p.Asn431Ser |
| ENST00000569217.1:n.601A>G | |
| XM_011545928.1:c.1208A>G | XP_011544230.1:p.Asn403Ser |