Linked Data
ClinVar Variation Id:
502269
dbSNP Id:
rs575064188
ExAC:
2:219677688 C / T
gnomAD v2:
2-219677688-C-T
gnomAD v3:
2-218812965-C-T
gnomAD v4:
2-218812965-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218812965C>T , CM000664.2:g.218812965C>T | GRCh38 |
| NC_000002.11:g.219677688C>T , CM000664.1:g.219677688C>T | GRCh37 |
| NC_000002.10:g.219385932C>T | NCBI36 |
| NG_007959.1:g.36217C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258415.9:c.886C>T MANE Select | ENSP00000258415.4:p.Gln296Ter | |
| ENST00000258415.8:c.886C>T | ENSP00000258415.4:p.Gln296Ter | |
| ENST00000411688.1:c.604C>T | ENSP00000392671.1:p.Gln202Ter | |
| ENST00000445971.1:c.*347C>T | ENSP00000404945.1:n.*347C>T | |
| ENST00000466602.1:n.1008C>T | ||
| ENST00000494263.5:n.1320C>T | ||
| NM_000784.3:c.886C>T | NP_000775.1:p.Gln296Ter | |
| XM_017003488.2:c.466C>T | XP_016858977.1:p.Gln156Ter | |
| NM_000784.4:c.886C>T MANE Select | NP_000775.1:p.Gln296Ter |