Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154956961T= , CM000685.2:g.154956961T= | GRCh38 |
| NC_000023.10:g.154185236T= , CM000685.1:g.154185236T= | GRCh37 |
| NC_000023.9:g.153838430T= | NCBI36 |
| NG_011403.1:g.70763A= | |
| NG_011403.2:g.70763A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.1748A= MANE Select | ENSP00000353393.4:p.Asn583= | |
| ENST00000647125.1:c.*1624A= | ENSP00000496062.1:n.*1624A= | |
| ENST00000360256.8:c.1748A= | ENSP00000353393.4:p.Asn583= | |
| NM_000132.3:c.1748A= | NP_000123.1:p.Asn583= | |
| XM_011531126.1:c.1643A= | XP_011529428.1:p.Asn548= | |
| NM_000132.4:c.1748A= MANE Select | NP_000123.1:p.Asn583= |