Linked Data
dbSNP Id:
rs1812590129
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.118947891G>C , CM000670.2:g.118947891G>C | GRCh38 |
| NC_000008.10:g.119960130G>C , CM000670.1:g.119960130G>C | GRCh37 |
| NC_000008.9:g.120029311G>C | NCBI36 |
| NG_012202.1:g.9254C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297350.9:c.30+3901C>G MANE Select | ENSP00000297350.4:n.30+3901C>G | |
| ENST00000297350.8:c.30+3901C>G | ENSP00000297350.4:n.30+3901C>G | |
| ENST00000517352.1:c.30+3901C>G | ENSP00000427924.1:n.30+3901C>G | |
| NM_002546.3:c.30+3901C>G | NP_002537.3:n.30+3901C>G | |
| NM_002546.4:c.30+3901C>G MANE Select | NP_002537.3:n.30+3901C>G |