Linked Data
dbSNP Id:
rs1575077681
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232484766A>C , CM000664.2:g.232484766A>C | GRCh38 |
| NC_000002.11:g.233349476A>C , CM000664.1:g.233349476A>C | GRCh37 |
| NC_000002.10:g.233057720A>C | NCBI36 |
| NG_034065.1:g.8094T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304546.6:c.1059+35T>G MANE Select | ENSP00000302051.1:n.1059+35T>G | |
| ENST00000304546.5:c.1059+35T>G | ENSP00000302051.1:n.1059+35T>G | |
| ENST00000409941.1:c.1059+35T>G | ENSP00000386333.1:n.1059+35T>G | |
| ENST00000482346.1:n.1370+35T>G | ||
| NM_001290787.1:c.1059+35T>G | NP_001277716.1:n.1059+35T>G | |
| NM_004826.3:c.1059+35T>G | NP_004817.2:n.1059+35T>G | |
| NM_004826.4:c.1059+35T>G MANE Select | NP_004817.2:n.1059+35T>G | |
| NM_001290787.2:c.1059+35T>G | NP_001277716.1:n.1059+35T>G |