Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32474895T>C , CM000684.2:g.32474895T>C | GRCh38 |
| NC_000022.10:g.32870882T>C , CM000684.1:g.32870882T>C | GRCh37 |
| NC_000022.9:g.31200882T>C | NCBI36 |
| NG_016001.1:g.5176T>C | |
| NG_016001.2:g.5176T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266087.12:c.-108T>C MANE Select | ENSP00000266087.7:n.-108T>C | |
| ENST00000266087.11:c.-108T>C | ENSP00000266087.7:n.-108T>C | |
| ENST00000420700.5:c.-108T>C | ENSP00000406155.1:n.-108T>C | |
| ENST00000425028.5:c.-108T>C | ENSP00000395823.1:n.-108T>C | |
| NM_012179.3:c.-108T>C | NP_036311.3:n.-108T>C | |
| XM_011530106.1:c.-281T>C | XP_011528408.1:n.-281T>C | |
| XM_024452207.1:c.-298T>C | XP_024307975.1:n.-298T>C | |
| NM_012179.4:c.-108T>C MANE Select | NP_036311.3:n.-108T>C |