Linked Data
gnomAD v4:
X-154379227-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154379227G>T , CM000685.2:g.154379227G>T | GRCh38 |
| NC_000023.10:g.153607587G>T , CM000685.1:g.153607587G>T | GRCh37 |
| NC_000023.9:g.153260781G>T | NCBI36 |
| NG_008677.1:g.9792G>T , LRG_745:g.9792G>T | |
| NG_011506.1:g.420C>A | |
| NG_011506.2:g.412C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369842.8:c.-258G>T | ENSP00000358857.4:n.-258G>T |