Linked Data
gnomAD v4:
5-132369705-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132369705G>T , CM000667.2:g.132369705G>T | GRCh38 |
| NC_000005.9:g.131705397G>T , CM000667.1:g.131705397G>T | GRCh37 |
| NC_000005.8:g.131733296G>T | NCBI36 |
| NG_008982.1:g.4997G>T | |
| NG_008982.2:g.5002G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_110997.1:n.73+139C>A (MIR3936HG) | ||
| XR_427718.1:n.2G>T (SLC22A5) | ||
| XR_948290.1:n.2G>T (SLC22A5) | ||
| XR_948291.1:n.2G>T (SLC22A5) | ||
| XR_001742215.1:n.2G>T (SLC22A5) | ||
| XR_001742216.1:n.2G>T (SLC22A5) | ||
| XR_427718.2:n.2G>T (SLC22A5) | ||
| XR_948290.2:n.2G>T (SLC22A5) | ||
| XR_948291.2:n.2G>T (SLC22A5) |