Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.8732071G= , CM000685.2:g.8732071G= | GRCh38 |
| NC_000023.10:g.8700112G= , CM000685.1:g.8700112G= | GRCh37 |
| NC_000023.9:g.8660112G= | NCBI36 |
| NG_007088.1:g.5116C= | |
| NG_007088.2:g.5116C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262648.8:c.-35C= MANE Select | ENSP00000262648.3:n.-35C= | |
| ENST00000262648.7:c.-35C= | ENSP00000262648.3:n.-35C= | |
| ENST00000619786.1:c.-35C= | ENSP00000478734.1:n.-35C= | |
| NM_000216.2:c.-35C= | NP_000207.2:n.-35C= | |
| XM_005274501.3:c.-35C= | XP_005274558.1:n.-35C= | |
| NM_000216.3:c.-35C= | NP_000207.2:n.-35C= | |
| XM_005274501.4:c.-35C= | XP_005274558.1:n.-35C= | |
| NM_000216.4:c.-35C= MANE Select | NP_000207.2:n.-35C= |