Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.74145292G= , CM000664.2:g.74145292G= | GRCh38 |
| NC_000002.11:g.74372419G= , CM000664.1:g.74372419G= | GRCh37 |
| NC_000002.10:g.74225927G= | NCBI36 |
| NG_031910.1:g.7621C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327428.10:c.66C= MANE Select | ENSP00000331369.5:p.His22= | |
| ENST00000295326.4:c.66C= | ENSP00000295326.4:p.His22= | |
| ENST00000327428.9:c.66C= | ENSP00000331369.5:p.His22= | |
| ENST00000469676.1:n.1089C= | ||
| ENST00000477685.5:n.217C= | ||
| ENST00000484655.1:n.2621C= | ||
| NM_001035505.1:c.66C= | NP_001030582.1:p.His22= | |
| NM_212552.2:c.66C= | NP_997717.2:p.His22= | |
| NM_212552.3:c.66C= MANE Select | NP_997717.2:p.His22= | |
| NM_001035505.2:c.66C= | NP_001030582.1:p.His22= |