Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.10309584G>T , CM000679.2:g.10309584G>T | GRCh38 |
| NC_000017.10:g.10212901G>T , CM000679.1:g.10212901G>T | GRCh37 |
| NC_000017.9:g.10153626G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003802.3:c.4903C>A MANE Select | NP_003793.2:p.His1635Asn |
| ENST00000252172.9:c.4903C>A MANE Select | ENSP00000252172.4:p.His1635Asn |
| NM_003802.2:c.4903C>A | NP_003793.2:p.His1635Asn |
| ENST00000252172.8:c.4903C>A | ENSP00000252172.4:p.His1635Asn |
| ENST00000418404.7:c.4903C>A | ENSP00000404570.3:p.His1635Asn |
| ENST00000418404.8:c.4903C>A | ENSP00000404570.3:p.His1635Asn |
| ENST00000621918.1:c.4903C>A | ENSP00000480864.1:p.His1635Asn |