Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.123218675A= , CM000668.2:g.123218675A= | GRCh38 |
| NC_000006.11:g.123539820A= , CM000668.1:g.123539820A= | GRCh37 |
| NC_000006.10:g.123581519A= | NCBI36 |
| NG_030438.1:g.423419T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000334268.9:c.2116T= MANE Select | ENSP00000333984.5:p.Phe706= | |
| ENST00000334268.8:c.2116T= | ENSP00000333984.5:p.Phe706= | |
| NM_006073.3:c.2116T= | NP_006064.2:p.Phe706= | |
| XM_011535382.1:c.2035T= | XP_011533684.1:p.Phe679= | |
| NM_006073.4:c.2116T= MANE Select | NP_006064.2:p.Phe706= |