Linked Data
gnomAD v4:
2-240868591-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240868591G>T , CM000664.2:g.240868591G>T | GRCh38 |
| NC_000002.11:g.241808008G>T , CM000664.1:g.241808008G>T | GRCh37 |
| NC_000002.10:g.241456681G>T | NCBI36 |
| NG_008005.1:g.4847G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.3:c.-275G>T | ENSP00000302620.3:n.-275G>T | |
| XR_924060.1:n.405+1642C>A |