Linked Data
MyVariant Identifiers:
chr8:g.24814057C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.24956543C>A , CM000670.2:g.24956543C>A | GRCh38 |
| NC_000008.10:g.24814057C>A , CM000670.1:g.24814057C>A | GRCh37 |
| NC_000008.9:g.24869974C>A | NCBI36 |
| NG_008492.1:g.5075G>T , LRG_259:g.5075G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000610854.2:c.-28G>T MANE Select | ENSP00000482169.2:n.-28G>T | |
| ENST00000610854.1:c.-28G>T | ENSP00000482169.1:n.-28G>T | |
| ENST00000615973.1:n.179G>T | ||
| ENST00000619417.1:c.-28G>T | ENSP00000483690.1:n.-28G>T | |
| NM_006158.4:c.-28G>T , LRG_259t1:c.-28G>T | NP_006149.2:n.-28G>T | |
| NM_006158.5:c.-28G>T MANE Select | NP_006149.2:n.-28G>T |