Linked Data
dbSNP Id:
rs756686
gnomAD v2:
9-136135503-G-A
gnomAD v3:
9-133260099-G-A
gnomAD v4:
9-133260099-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133260099G>A , CM000671.2:g.133260099G>A | GRCh38 |
| NC_000009.11:g.136135503G>A , CM000671.1:g.136135503G>A | GRCh37 |
| NC_000009.10:g.135125324G>A | NCBI36 |
| NG_006669.1:g.17551C>T | |
| NG_006669.2:g.20116C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.186-233C>T | ||
| ENST00000647353.1:n.54-8947C>T | ||
| ENST00000651471.1:n.191-233C>T | ||
| ENST00000679909.1:c.28+15063C>T | ENSP00000506089.1:n.28+15063C>T | |
| ENST00000453660.3:n.168-233C>T | ||
| ENST00000538324.2:c.156-233C>T | ENSP00000483018.1:n.156-233C>T | |
| ENST00000611156.4:c.156-233C>T | ENSP00000483265.1:n.156-233C>T | |
| NM_020469.2:c.156-233C>T | NP_065202.2:n.156-233C>T | |
| NM_020469.3:c.156-233C>T | NP_065202.2:n.156-233C>T |