Linked Data
dbSNP Id:
rs1567504885
gnomAD v2:
16-88876850-T-C
gnomAD v4:
16-88810442-T-C
MyVariant Identifiers:
chr16:g.88876850T>C (hg19)
chr16:g.88876850_88876853delinsCAGG (hg19)
chr16:g.88810442T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88810442T>C , CM000678.2:g.88810442T>C | GRCh38 |
| NC_000016.9:g.88876850T>C , CM000678.1:g.88876850T>C | GRCh37 |
| NC_000016.8:g.87404351T>C | NCBI36 |
| NG_008013.1:g.6493A>G | |
| NG_028266.1:g.11665T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378364.8:c.302A>G MANE Select | ENSP00000367615.3:p.Tyr101Cys | |
| ENST00000378364.7:c.302A>G | ENSP00000367615.3:p.Tyr101Cys | |
| ENST00000426324.6:c.302A>G | ENSP00000397007.2:p.Tyr101Cys | |
| ENST00000562464.1:n.332-294A>G | ||
| ENST00000563655.5:c.241-294A>G | ENSP00000456012.1:n.241-294A>G | |
| ENST00000567391.5:c.188-294A>G | ENSP00000457964.1:n.188-294A>G | |
| ENST00000567713.5:c.302A>G | ENSP00000455749.1:p.Tyr101Cys | |
| ENST00000568319.5:c.188-294A>G | ENSP00000456905.1:n.188-294A>G | |
| ENST00000569616.1:c.300A>G | ||
| NM_000485.2:c.302A>G | NP_000476.1:p.Tyr101Cys | |
| NM_001030018.1:c.302A>G | NP_001025189.1:p.Tyr101Cys | |
| NM_000485.3:c.302A>G MANE Select | NP_000476.1:p.Tyr101Cys | |
| NM_001030018.2:c.302A>G | NP_001025189.1:p.Tyr101Cys |