Linked Data
gnomAD v3:
8-86739665-G-T
gnomAD v4:
8-86739665-G-T
MyVariant Identifiers:
chr8:g.87751893G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86739665G>T , CM000670.2:g.86739665G>T | GRCh38 |
| NC_000008.10:g.87751893G>T , CM000670.1:g.87751893G>T | GRCh37 |
| NC_000008.9:g.87821009G>T | NCBI36 |
| NG_016980.1:g.9011C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.201C>A MANE Select | ENSP00000316605.5:p.Thr67= | |
| ENST00000681746.1:c.201C>A | ENSP00000505959.1:p.Thr67= | |
| ENST00000320005.5:c.201C>A | ENSP00000316605.5:p.Thr67= | |
| ENST00000519777.1:n.183C>A | ||
| NM_019098.4:c.201C>A | NP_061971.3:p.Thr67= | |
| NM_019098.5:c.201C>A MANE Select | NP_061971.3:p.Thr67= |