Linked Data
gnomAD v4:
5-172333466-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.172333466C>A , CM000667.2:g.172333466C>A | GRCh38 |
| NC_000005.9:g.171760470C>A , CM000667.1:g.171760470C>A | GRCh37 |
| NC_000005.8:g.171693075C>A | NCBI36 |
| NG_027746.1:g.126058G>T | |
| NG_027746.2:g.126058G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000636523.1:c.1229-8086G>T | ||
| ENST00000519643.5:c.1189-8086G>T | ENSP00000430890.1:n.1189-8086G>T | |
| NM_001308175.1:c.1189-8086G>T | NP_001295104.1:n.1189-8086G>T | |
| NM_001308175.2:c.1189-8086G>T | NP_001295104.1:n.1189-8086G>T |