Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.955229A>G , CM000674.2:g.955229A>G | GRCh38 |
| NC_000012.11:g.1064395A>G , CM000674.1:g.1064395A>G | GRCh37 |
| NC_000012.10:g.934656A>G | NCBI36 |
| NG_017078.2:g.39813T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000430095.6:c.-18-22153T>C | ENSP00000387901.2:n.-18-22153T>C | |
| NM_001297419.1:c.-18-22153T>C | NP_001284348.1:n.-18-22153T>C | |
| XM_005253720.3:c.-18-22153T>C | XP_005253777.1:n.-18-22153T>C | |
| XM_005253720.5:c.-18-22153T>C | XP_005253777.1:n.-18-22153T>C | |
| XM_017019769.1:c.-18-22153T>C | XP_016875258.1:n.-18-22153T>C |