Linked Data
gnomAD v4:
X-154097849-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154097849G>T , CM000685.2:g.154097849G>T | GRCh38 |
| NC_000023.10:g.153363306G>T , CM000685.1:g.153363306G>T | GRCh37 |
| NC_000023.9:g.153016500G>T | NCBI36 |
| NG_007107.2:g.44273C>A | |
| NG_007107.3:g.44255C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000631210.1:n.305+6932C>A |