Linked Data
ClinVar Variation Id:
100395
dbSNP Id:
rs61750580
gnomAD v2:
12-6127759-C-T
gnomAD v4:
12-6018593-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6018593C>T , CM000674.2:g.6018593C>T | GRCh38 |
| NC_000012.11:g.6127759C>T , CM000674.1:g.6127759C>T | GRCh37 |
| NC_000012.10:g.5998020C>T | NCBI36 |
| NG_009072.1:g.111078G>A | |
| NG_009072.2:g.111078G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261405.10:c.4825G>A MANE Select | ENSP00000261405.5:p.Gly1609Arg | |
| ENST00000261405.9:c.4825G>A | ENSP00000261405.5:p.Gly1609Arg | |
| ENST00000538635.5:n.421-24659G>A | ||
| NM_000552.3:c.4825G>A | NP_000543.2:p.Gly1609Arg | |
| NM_000552.4:c.4825G>A | NP_000543.2:p.Gly1609Arg | |
| NM_000552.5:c.4825G>A MANE Select | NP_000543.3:p.Gly1609Arg |