Linked Data
dbSNP Id:
rs2120108503
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.69647983T>A , CM000673.2:g.69647983T>A | GRCh38 |
| NC_000011.9:g.69462751T>A , CM000673.1:g.69462751T>A | GRCh37 |
| NC_000011.8:g.69171932T>A | NCBI36 |
| NG_007375.1:g.11879T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227507.3:c.575-11T>A MANE Select | ENSP00000227507.2:n.575-11T>A | |
| ENST00000227507.2:c.575-11T>A | ENSP00000227507.2:n.575-11T>A | |
| ENST00000536559.1:c.199-11T>A | ENSP00000438482.1:n.199-11T>A | |
| ENST00000542367.1:n.27T>A | ||
| ENST00000545484.1:n.281-11T>A | ||
| NM_053056.2:c.575-11T>A | NP_444284.1:n.575-11T>A | |
| XM_006718653.2:c.599-11T>A | XP_006718716.1:n.599-11T>A | |
| NM_053056.3:c.575-11T>A MANE Select | NP_444284.1:n.575-11T>A |