Linked Data
dbSNP Id:
rs2124200356
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.16132092T>C , CM000663.2:g.16132092T>C | GRCh38 |
| NC_000001.10:g.16458587T>C , CM000663.1:g.16458587T>C | GRCh37 |
| NC_000001.9:g.16331174T>C | NCBI36 |
| NG_021396.1:g.28996A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358432.8:c.2297A>G MANE Select | ENSP00000351209.5:p.Asp766Gly | |
| ENST00000358432.7:c.2297A>G | ENSP00000351209.5:p.Asp766Gly | |
| NM_004431.3:c.2297A>G | NP_004422.2:p.Asp766Gly | |
| NM_001329090.1:c.2135A>G | NP_001316019.1:p.Asp712Gly | |
| NM_004431.4:c.2297A>G | NP_004422.2:p.Asp766Gly | |
| NM_004431.5:c.2297A>G MANE Select | NP_004422.2:p.Asp766Gly | |
| NM_001329090.2:c.2135A>G | NP_001316019.1:p.Asp712Gly |