Linked Data
MyVariant Identifiers:
chr8:g.87683269T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86671041T>G , CM000670.2:g.86671041T>G | GRCh38 |
| NC_000008.10:g.87683269T>G , CM000670.1:g.87683269T>G | GRCh37 |
| NC_000008.9:g.87752385T>G | NCBI36 |
| NG_016980.1:g.77635A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.396A>C MANE Select | ENSP00000316605.5:p.Leu132= | |
| ENST00000680314.1:n.157A>C | ||
| ENST00000681746.1:c.396A>C | ENSP00000505959.1:p.Leu132= | |
| ENST00000320005.5:c.396A>C | ENSP00000316605.5:p.Leu132= | |
| NM_019098.4:c.396A>C | NP_061971.3:p.Leu132= | |
| XM_011517138.1:c.-19A>C | XP_011515440.1:n.-19A>C | |
| XM_011517138.2:c.-19A>C | XP_011515440.1:n.-19A>C | |
| NM_019098.5:c.396A>C MANE Select | NP_061971.3:p.Leu132= |