Linked Data
dbSNP Id:
rs1939197266
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.53973842G>A , CM000674.2:g.53973842G>A | GRCh38 |
| NC_000012.11:g.54367626G>A , CM000674.1:g.54367626G>A | GRCh37 |
| NC_000012.10:g.52653893G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000243082.4:c.601G>A (HOXC11) | ENSP00000243082.4:p.Ala201Thr | |
| ENST00000546378.1:c.601G>A (HOXC11) MANE Select | ENSP00000446680.1:p.Ala201Thr | |
| NM_014212.3:c.601G>A (HOXC11) | NP_055027.1:p.Ala201Thr | |
| NR_047517.1:n.59+1056C>T (HOTAIR) | ||
| NM_014212.4:c.601G>A (HOXC11) MANE Select | NP_055027.1:p.Ala201Thr |