Linked Data
MyVariant Identifiers:
chr8:g.24809968G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.24952455G>A , CM000670.2:g.24952455G>A | GRCh38 |
| NC_000008.10:g.24809968G>A , CM000670.1:g.24809968G>A | GRCh37 |
| NC_000008.9:g.24865885G>A | NCBI36 |
| NG_008492.1:g.9163C>T , LRG_259:g.9163C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000610854.2:c.*355C>T MANE Select | ENSP00000482169.2:n.*355C>T | |
| ENST00000610854.1:c.*355C>T | ENSP00000482169.1:n.*355C>T | |
| ENST00000619417.1:c.*852C>T | ENSP00000483690.1:n.*852C>T | |
| NM_006158.4:c.*355C>T , LRG_259t1:c.*355C>T | NP_006149.2:n.*355C>T | |
| NM_006158.5:c.*355C>T MANE Select | NP_006149.2:n.*355C>T |