Linked Data
dbSNP Id:
rs1442849
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8120803C>G , CM000679.2:g.8120803C>G | GRCh38 |
| NC_000017.10:g.8024121C>G , CM000679.1:g.8024121C>G | GRCh37 |
| NC_000017.9:g.7964846C>G | NCBI36 |
| NG_015807.1:g.3114G>C | |
| NG_015816.1:g.8290G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000541682.7:c.*768G>C MANE Select | ENSP00000446205.2:n.*768G>C | |
| ENST00000541682.6:c.1461G>C | ENSP00000446205.2:n.1461G>C | |
| NM_001165967.1:c.*768G>C | NP_001159439.1:n.*768G>C | |
| NM_032580.3:c.*768G>C | NP_115969.2:n.*768G>C | |
| XM_011524038.1:c.*768G>C | XP_011522340.1:n.*768G>C | |
| XR_934203.1:n.69+989C>G | ||
| XM_017025232.1:c.*768G>C | XP_016880721.1:n.*768G>C | |
| XM_024451007.1:c.*768G>C | XP_024306775.1:n.*768G>C | |
| NM_001165967.2:c.*768G>C MANE Select | NP_001159439.1:n.*768G>C | |
| NM_032580.4:c.*768G>C | NP_115969.2:n.*768G>C |