Linked Data
MyVariant Identifiers:
chr8:g.24810157A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.24952644A>T , CM000670.2:g.24952644A>T | GRCh38 |
| NC_000008.10:g.24810157A>T , CM000670.1:g.24810157A>T | GRCh37 |
| NC_000008.9:g.24866074A>T | NCBI36 |
| NG_008492.1:g.8974T>A , LRG_259:g.8974T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000610854.2:c.*166T>A MANE Select | ENSP00000482169.2:n.*166T>A | |
| ENST00000610854.1:c.*166T>A | ENSP00000482169.1:n.*166T>A | |
| ENST00000619417.1:c.*663T>A | ENSP00000483690.1:n.*663T>A | |
| NM_006158.4:c.*166T>A , LRG_259t1:c.*166T>A | NP_006149.2:n.*166T>A | |
| NM_006158.5:c.*166T>A MANE Select | NP_006149.2:n.*166T>A |