Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.36701528C= , CM000684.2:g.36701528C= | GRCh38 |
| NC_000022.10:g.37097573C= , CM000684.1:g.37097573C= | GRCh37 |
| NC_000022.9:g.35427519C= | NCBI36 |
| NG_031861.1:g.6118G= | |
| NG_031861.2:g.6331G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300105.7:c.211+838G= MANE Select | ENSP00000300105.6:n.211+838G= | |
| ENST00000300105.6:c.211+838G= | ENSP00000300105.6:n.211+838G= | |
| NM_006078.3:c.211+838G= | NP_006069.1:n.211+838G= | |
| NM_006078.4:c.211+838G= | NP_006069.1:n.211+838G= | |
| NM_001379051.1:c.142+838G= | NP_001365980.1:n.142+838G= | |
| NM_006078.5:c.211+838G= MANE Select | NP_006069.1:n.211+838G= | |
| NR_166440.1:n.1387+838G= |