Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.206110180G= , CM000663.2:g.206110180G= | GRCh38 |
| NC_000001.10:g.206231151C= , CM000663.1:g.206231151C= | GRCh37 |
| NC_000001.9:g.204397774C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367126.5:c.*9C= MANE Select | ENSP00000356094.4:n.*9C= | |
| ENST00000367126.4:c.*9C= | ENSP00000356094.4:n.*9C= | |
| ENST00000612906.1:n.380C= | ||
| NM_000707.3:c.*9C= | NP_000698.1:n.*9C= | |
| NM_000707.4:c.*9C= | NP_000698.1:n.*9C= | |
| NM_000707.5:c.*9C= MANE Select | NP_000698.1:n.*9C= |