Linked Data
dbSNP Id:
rs1270199779
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19955589T>A , CM000670.2:g.19955589T>A | GRCh38 |
| NC_000008.10:g.19813100T>A , CM000670.1:g.19813100T>A | GRCh37 |
| NC_000008.9:g.19857380T>A | NCBI36 |
| NG_008855.1:g.21519T>A | |
| NG_008855.2:g.58873T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000650287.1:c.776-252T>A MANE Select | ENSP00000497642.1:n.776-252T>A | |
| ENST00000311322.8:c.776-252T>A | ENSP00000309757.6:n.776-252T>A | |
| NM_000237.2:c.776-252T>A | NP_000228.1:n.776-252T>A | |
| NM_000237.3:c.776-252T>A MANE Select | NP_000228.1:n.776-252T>A |