Linked Data
gnomAD v4:
12-91111543-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.91111543C>T , CM000674.2:g.91111543C>T | GRCh38 |
| NC_000012.11:g.91505320C>T , CM000674.1:g.91505320C>T | GRCh37 |
| NC_000012.10:g.90029451C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266718.4:c.-167G>A | ENSP00000266718.4:n.-167G>A | |
| NM_002345.3:c.-167G>A | NP_002336.1:n.-167G>A |