Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32474732G= , CM000684.2:g.32474732G= | GRCh38 |
| NC_000022.10:g.32870719G= , CM000684.1:g.32870719G= | GRCh37 |
| NC_000022.9:g.31200719G= | NCBI36 |
| NG_016001.1:g.5013G= | |
| NG_016001.2:g.5013G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266087.11:c.-271G= | ENSP00000266087.7:n.-271G= | |
| ENST00000420700.5:c.-271G= | ENSP00000406155.1:n.-271G= | |
| NM_012179.3:c.-271G= | NP_036311.3:n.-271G= | |
| XM_011530106.1:c.-444G= | XP_011528408.1:n.-444G= | |
| XM_024452207.1:c.-461G= | XP_024307975.1:n.-461G= |