Linked Data
dbSNP Id:
rs574347
gnomAD v3:
9-133260255-T-C
gnomAD v4:
9-133260255-T-C
MyVariant Identifiers:
chr9:g.133260255T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133260255T>C , CM000671.2:g.133260255T>C | GRCh38 |
| NG_006669.1:g.17395A>G | |
| NG_006669.2:g.19960A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000453660.4:n.186-389A>G | ||
| ENST00000647353.1:n.54-9103A>G | ||
| ENST00000651471.1:n.191-389A>G | ||
| ENST00000679909.1:c.28+14907A>G | ENSP00000506089.1:n.28+14907A>G | |
| ENST00000453660.3:n.168-389A>G | ||
| ENST00000538324.2:c.156-389A>G | ENSP00000483018.1:n.156-389A>G | |
| ENST00000611156.4:c.156-389A>G | ENSP00000483265.1:n.156-389A>G | |
| NM_020469.2:c.156-389A>G | NP_065202.2:n.156-389A>G | |
| NM_020469.3:c.156-389A>G | NP_065202.2:n.156-389A>G |