Linked Data
MyVariant Identifiers:
chr8:g.65528615T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.64616058T>C , CM000670.2:g.64616058T>C | GRCh38 |
| NC_000008.10:g.65528615T>C , CM000670.1:g.65528615T>C | GRCh37 |
| NC_000008.9:g.65691169T>C | NCBI36 |
| NG_008338.1:g.187734A>G | |
| NG_008338.2:g.187734A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310193.4:c.483A>G MANE Select | ENSP00000310721.3:p.Leu161= | |
| ENST00000310193.3:c.483A>G | ENSP00000310721.3:p.Leu161= | |
| NM_004820.3:c.483A>G | NP_004811.1:p.Leu161= | |
| NM_001324112.1:c.483A>G | NP_001311041.1:p.Leu161= | |
| NM_004820.4:c.483A>G | NP_004811.1:p.Leu161= | |
| XM_017014002.1:c.549A>G | XP_016869491.1:p.Leu183= | |
| NM_004820.5:c.483A>G MANE Select | NP_004811.1:p.Leu161= | |
| NM_001324112.2:c.483A>G | NP_001311041.1:p.Leu161= |