Linked Data
gnomAD v4:
X-46836997-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.46836997G>T , CM000685.2:g.46836997G>T | GRCh38 |
| NC_000023.10:g.46696432G>T , CM000685.1:g.46696432G>T | GRCh37 |
| NC_000023.9:g.46581376G>T | NCBI36 |
| NG_009107.1:g.5086G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218340.3:c.-104G>T | ENSP00000218340.3:n.-104G>T | |
| NM_006915.2:c.-104G>T | NP_008846.2:n.-104G>T |