Linked Data
dbSNP Id:
rs113986870
gnomAD v2:
17-44355683-G-A
gnomAD v3:
17-46278317-G-A
gnomAD v4:
17-46278317-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.46278317G>A , CM000679.2:g.46278317G>A | GRCh38 |
| NC_000017.10:g.44355683G>A , CM000679.1:g.44355683G>A | GRCh37 |
| NC_000017.9:g.41711460G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000705759.1:n.377-2899C>T (ARL17B) | ||
| ENST00000570618.5:c.*22-2899C>T (ARL17B) | ENSP00000459151.1:n.*22-2899C>T | |
| XM_005256918.3:c.*22-2899C>T (ARL17B) | XP_005256975.1:n.*22-2899C>T | |
| XM_005257887.3:c.27-21477G>A (LRRC37A) | XP_005257944.1:n.27-21477G>A | |
| XM_011524162.1:c.*54-2899C>T (ARL17B) | XP_011522464.1:n.*54-2899C>T | |
| XM_011525540.1:c.27-21477G>A (LRRC37A) | XP_011523842.1:n.27-21477G>A | |
| NM_001103154.2:c.*22-2899C>T (ARL17B) | NP_001096624.1:n.*22-2899C>T | |
| XM_011524162.3:c.*54-2899C>T (ARL17B) | XP_011522464.1:n.*54-2899C>T |