Linked Data
dbSNP Id:
rs1575975069
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.87259718A>G , CM000665.2:g.87259718A>G | GRCh38 |
| NC_000003.11:g.87308868A>G , CM000665.1:g.87308868A>G | GRCh37 |
| NC_000003.10:g.87391558A>G | NCBI36 |
| NG_008225.2:g.21870T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344265.8:c.*176T>C | ENSP00000342931.3:n.*176T>C | |
| ENST00000350375.7:c.*176T>C MANE Select | ENSP00000263781.2:n.*176T>C | |
| ENST00000350375.6:c.*176T>C | ENSP00000263781.2:n.*176T>C | |
| NM_000306.3:c.*176T>C | NP_000297.1:n.*176T>C | |
| NM_001122757.2:c.*176T>C | NP_001116229.1:n.*176T>C | |
| NM_000306.4:c.*176T>C MANE Select | NP_000297.1:n.*176T>C | |
| NM_001122757.3:c.*176T>C | NP_001116229.1:n.*176T>C |