Linked Data
dbSNP Id:
rs755958174
ExAC:
11:124742384 C / T
gnomAD v2:
11-124742384-C-T
gnomAD v3:
11-124872488-C-T
gnomAD v4:
11-124872488-C-T
MyVariant Identifiers:
chr11:g.124742384C>T (hg19)
chr11:g.124742384_124742386delinsTGT (hg19)
chr11:g.124872488C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.124872488C>T , CM000673.2:g.124872488C>T | GRCh38 |
| NC_000011.9:g.124742384C>T , CM000673.1:g.124742384C>T | GRCh37 |
| NC_000011.8:g.124247594C>T | NCBI36 |
| NG_016214.1:g.12080C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397801.6:c.1266C>T MANE Select | ENSP00000380903.1:p.Tyr422= | |
| ENST00000397801.5:c.1266C>T | ENSP00000380903.1:p.Tyr422= | |
| ENST00000538940.5:c.1200C>T | ENSP00000441797.1:p.Tyr400= | |
| NM_022370.3:c.1266C>T | NP_071765.2:p.Tyr422= | |
| XM_011542953.1:c.2238C>T | XP_011541255.1:p.Tyr746= | |
| XM_017018122.1:c.1200C>T | XP_016873611.1:p.Tyr400= | |
| NM_022370.4:c.1266C>T MANE Select | NP_071765.2:p.Tyr422= |