Linked Data
dbSNP Id:
rs921372384
gnomAD v3:
9-133261705-C-T
gnomAD v4:
9-133261705-C-T
MyVariant Identifiers:
chr9:g.133261705C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133261705C>T , CM000671.2:g.133261705C>T | GRCh38 |
| NC_000009.11:g.136137108C>T , CM000671.1:g.136137108C>T | GRCh37 |
| NC_000009.10:g.135126929C>T | NCBI36 |
| NG_006669.1:g.15945G>A | |
| NG_006669.2:g.18510G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.129-331G>A | ||
| ENST00000647353.1:n.54-10553G>A | ||
| ENST00000651471.1:n.134-331G>A | ||
| ENST00000679909.1:c.28+13457G>A | ENSP00000506089.1:n.28+13457G>A | |
| ENST00000453660.3:n.111-331G>A | ||
| ENST00000538324.2:c.99-331G>A | ENSP00000483018.1:n.99-331G>A | |
| ENST00000611156.4:c.99-331G>A | ENSP00000483265.1:n.99-331G>A | |
| NM_020469.2:c.99-331G>A | NP_065202.2:n.99-331G>A | |
| NM_020469.3:c.99-331G>A | NP_065202.2:n.99-331G>A |