Linked Data
MyVariant Identifiers:
chr8:g.24814122T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.24956608T>C , CM000670.2:g.24956608T>C | GRCh38 |
| NC_000008.10:g.24814122T>C , CM000670.1:g.24814122T>C | GRCh37 |
| NC_000008.9:g.24870039T>C | NCBI36 |
| NG_008492.1:g.5010A>G , LRG_259:g.5010A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000610854.2:c.-93A>G MANE Select | ENSP00000482169.2:n.-93A>G | |
| ENST00000610854.1:c.-93A>G | ENSP00000482169.1:n.-93A>G | |
| ENST00000615973.1:n.114A>G | ||
| ENST00000619417.1:c.-93A>G | ENSP00000483690.1:n.-93A>G | |
| NM_006158.4:c.-93A>G , LRG_259t1:c.-93A>G | NP_006149.2:n.-93A>G | |
| NM_006158.5:c.-93A>G MANE Select | NP_006149.2:n.-93A>G |