Linked Data
dbSNP Id:
rs1259489828
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218881894C>G , CM000664.2:g.218881894C>G | GRCh38 |
| NC_000002.11:g.219746616C>G , CM000664.1:g.219746616C>G | GRCh37 |
| NC_000002.10:g.219454860C>G | NCBI36 |
| NG_012179.1:g.6362C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258411.8:c.114-267C>G MANE Select | ENSP00000258411.3:n.114-267C>G | |
| ENST00000258411.7:c.114-267C>G | ENSP00000258411.3:n.114-267C>G | |
| NM_025216.2:c.114-267C>G | NP_079492.2:n.114-267C>G | |
| XM_011511928.1:c.63-267C>G | XP_011510230.1:n.63-267C>G | |
| XM_011511929.1:c.18-267C>G | XP_011510231.1:n.18-267C>G | |
| XM_011511930.1:c.114-267C>G | XP_011510232.1:n.114-267C>G | |
| XM_011511929.2:c.18-267C>G | XP_011510231.1:n.18-267C>G | |
| NM_025216.3:c.114-267C>G MANE Select | NP_079492.2:n.114-267C>G |