Linked Data
dbSNP Id:
rs10849138
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4754142G>A , CM000674.2:g.4754142G>A | GRCh38 |
| NC_000012.11:g.4863308G>A , CM000674.1:g.4863308G>A | GRCh37 |
| NC_000012.10:g.4733569G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000252318.7:c.1174-6816G>A MANE Select | ENSP00000252318.2:n.1174-6816G>A | |
| ENST00000648836.1:c.964-6816G>A | ENSP00000497305.1:n.964-6816G>A | |
| ENST00000648865.1:n.26-6816G>A | ||
| ENST00000252318.6:c.1174-6816G>A | ENSP00000252318.2:n.1174-6816G>A | |
| NM_017417.1:c.1174-6816G>A | NP_059113.1:n.1174-6816G>A | |
| NM_017417.2:c.1174-6816G>A MANE Select | NP_059113.1:n.1174-6816G>A |