Linked Data
dbSNP Id:
rs182985414
gnomAD v2:
9-136133346-A-C
gnomAD v3:
9-133257959-A-C
gnomAD v4:
9-133257959-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133257959A>C , CM000671.2:g.133257959A>C | GRCh38 |
| NC_000009.11:g.136133346A>C , CM000671.1:g.136133346A>C | GRCh37 |
| NC_000009.10:g.135123167A>C | NCBI36 |
| NG_006669.1:g.19708T>G | |
| NG_006669.2:g.22256T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.269+138T>G | ||
| ENST00000647353.1:n.54-6807T>G | ||
| ENST00000651471.1:n.329+83T>G | ||
| ENST00000679909.1:c.28+17203T>G | ENSP00000506089.1:n.28+17203T>G | |
| ENST00000453660.3:n.251+138T>G | ||
| ENST00000538324.2:c.239+138T>G | ENSP00000483018.1:n.239+138T>G | |
| ENST00000611156.4:c.239+138T>G | ENSP00000483265.1:n.239+138T>G | |
| NM_020469.2:c.239+138T>G | NP_065202.2:n.239+138T>G | |
| NM_020469.3:c.239+138T>G | NP_065202.2:n.239+138T>G |