Linked Data
dbSNP Id:
rs1807822800
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.95318448G>A , CM000669.2:g.95318448G>A | GRCh38 |
| NC_000007.13:g.94947760G>A , CM000669.1:g.94947760G>A | GRCh37 |
| NC_000007.12:g.94785696G>A | NCBI36 |
| NG_008779.1:g.11125C>T | |
| NG_008779.2:g.11259C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222381.8:c.75-55C>T MANE Select | ENSP00000222381.3:n.75-55C>T | |
| ENST00000222381.7:c.75-55C>T | ENSP00000222381.3:n.75-55C>T | |
| ENST00000433729.1:c.75-55C>T | ENSP00000407359.1:n.75-55C>T | |
| ENST00000470502.1:n.140C>T | ||
| NM_000446.5:c.75-55C>T | NP_000437.3:n.75-55C>T | |
| NM_000446.6:c.75-55C>T | NP_000437.3:n.75-55C>T | |
| NM_000446.7:c.75-55C>T MANE Select | NP_000437.3:n.75-55C>T |