Linked Data
dbSNP Id:
rs1427966520
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110573498G>A , CM000672.2:g.110573498G>A | GRCh38 |
| NC_000010.10:g.112333256G>A , CM000672.1:g.112333256G>A | GRCh37 |
| NC_000010.9:g.112323246G>A | NCBI36 |
| NG_012217.1:g.10808G>A , LRG_774:g.10808G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.225-209G>A | ||
| ENST00000687823.1:n.45-1838G>A | ||
| ENST00000689932.1:n.356G>A | ||
| ENST00000691297.1:n.225-209G>A | ||
| ENST00000691527.1:n.182-209G>A | ||
| ENST00000692792.1:n.211-209G>A | ||
| ENST00000361804.5:c.92-209G>A MANE Select | ENSP00000354720.5:n.92-209G>A | |
| ENST00000361804.4:c.92-209G>A | ENSP00000354720.4:n.92-209G>A | |
| ENST00000462899.1:n.238-209G>A | ||
| NM_005445.3:c.92-209G>A , LRG_774t1:c.92-209G>A | NP_005436.1:n.92-209G>A | |
| NM_005445.4:c.92-209G>A MANE Select | NP_005436.1:n.92-209G>A |