Linked Data
dbSNP Id:
rs1855809832
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.69648193A>G , CM000673.2:g.69648193A>G | GRCh38 |
| NC_000011.9:g.69462961A>G , CM000673.1:g.69462961A>G | GRCh37 |
| NC_000011.8:g.69172142A>G | NCBI36 |
| NG_007375.1:g.12089A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227507.3:c.723+51A>G MANE Select | ENSP00000227507.2:n.723+51A>G | |
| ENST00000227507.2:c.723+51A>G | ENSP00000227507.2:n.723+51A>G | |
| ENST00000536559.1:c.*194A>G | ENSP00000438482.1:n.*194A>G | |
| ENST00000542367.1:n.186+51A>G | ||
| NM_053056.2:c.723+51A>G | NP_444284.1:n.723+51A>G | |
| XM_006718653.2:c.747+51A>G | XP_006718716.1:n.747+51A>G | |
| NM_053056.3:c.723+51A>G MANE Select | NP_444284.1:n.723+51A>G |