Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.219978562T>C , CM000663.2:g.219978562T>C | GRCh38 |
| NC_000001.10:g.220151904T>C , CM000663.1:g.220151904T>C | GRCh37 |
| NC_000001.9:g.218218527T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004446.3:c.4067A>G MANE Select | NP_004437.2:p.Asn1356Ser |
| ENST00000366923.8:c.4067A>G MANE Select | ENSP00000355890.3:p.Asn1356Ser |
| NM_004446.2:c.4067A>G | NP_004437.2:p.Asn1356Ser |
| ENST00000366923.7:c.4067A>G | ENSP00000355890.3:p.Asn1356Ser |
| XM_017000614.2:c.2489A>G | XP_016856103.1:p.Asn830Ser |