Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5227047A>C , CM000673.2:g.5227047A>C | GRCh38 |
| NC_000011.9:g.5248277A>C , CM000673.1:g.5248277A>C | GRCh37 |
| NC_000011.8:g.5204853A>C | NCBI36 |
| NG_000007.3:g.70569T>G | |
| NG_059281.1:g.5025T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.-26T>G | ENSP00000494175.1:n.-26T>G | |
| ENST00000335295.4:c.-26T>G MANE Select | ENSP00000333994.3:n.-26T>G | |
| ENST00000380315.2:c.-18-8T>G | ENSP00000369671.2:n.-18-8T>G | |
| ENST00000485743.1:n.26T>G | ||
| ENST00000633227.1:c.-26T>G | ENSP00000488004.1:n.-26T>G | |
| NM_000518.4:c.-26T>G | NP_000509.1:n.-26T>G | |
| NM_000518.5:c.-26T>G MANE Select | NP_000509.1:n.-26T>G |