Linked Data
dbSNP Id:
rs1886735835
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.75707434A>G , CM000676.2:g.75707434A>G | GRCh38 |
| NC_000014.8:g.76173777A>G , CM000676.1:g.76173777A>G | GRCh37 |
| NC_000014.7:g.75243530A>G | NCBI36 |
| NG_016974.1:g.51227A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000298832.14:c.656-189A>G MANE Select | ENSP00000298832.9:n.656-189A>G | |
| ENST00000286650.9:c.656-189A>G | ENSP00000286650.5:n.656-189A>G | |
| ENST00000298832.13:c.656-189A>G | ENSP00000298832.9:n.656-189A>G | |
| ENST00000555422.5:n.125-189A>G | ||
| ENST00000556173.5:n.582-189A>G | ||
| ENST00000557636.5:c.656-189A>G | ENSP00000450713.1:n.656-189A>G | |
| NM_015072.4:c.656-189A>G | NP_055887.3:n.656-189A>G | |
| NM_015072.5:c.656-189A>G MANE Select | NP_055887.3:n.656-189A>G |