Linked Data
dbSNP Id:
rs2303486
gnomAD v2:
17-46699669-A-T
gnomAD v3:
17-48622307-A-T
gnomAD v4:
17-48622307-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.48622307A>T , CM000679.2:g.48622307A>T | GRCh38 |
| NC_000017.10:g.46699669A>T , CM000679.1:g.46699669A>T | GRCh37 |
| NC_000017.9:g.44054668A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000311177.7:c.*593T>A (HOXB9) MANE Select | ENSP00000309439.5:n.*593T>A | |
| ENST00000311177.6:c.*593T>A (HOXB9) | ENSP00000309439.5:n.*593T>A | |
| ENST00000567101.2:n.59+11207T>A (HOXB7) | ||
| NM_024017.4:c.*593T>A (HOXB9) | NP_076922.1:n.*593T>A | |
| XM_011524728.1:c.517+3446T>A (HOXB9) | XP_011523030.1:n.517+3446T>A | |
| NM_024017.5:c.*593T>A (HOXB9) MANE Select | NP_076922.1:n.*593T>A |