Linked Data
gnomAD v4:
X-154379217-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154379217C>T , CM000685.2:g.154379217C>T | GRCh38 |
| NC_000023.10:g.153607577C>T , CM000685.1:g.153607577C>T | GRCh37 |
| NC_000023.9:g.153260771C>T | NCBI36 |
| NG_008677.1:g.9782C>T , LRG_745:g.9782C>T | |
| NG_011506.1:g.430G>A | |
| NG_011506.2:g.422G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369842.8:c.-268C>T | ENSP00000358857.4:n.-268C>T |