Linked Data
dbSNP Id:
rs1449013762
gnomAD v3:
9-133260303-T-A
gnomAD v4:
9-133260303-T-A
MyVariant Identifiers:
chr9:g.133260303T>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133260303T>A , CM000671.2:g.133260303T>A | GRCh38 |
| NC_000009.11:g.136135706T>A , CM000671.1:g.136135706T>A | GRCh37 |
| NC_000009.10:g.135125527T>A | NCBI36 |
| NG_006669.1:g.17347A>T | |
| NG_006669.2:g.19912A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000453660.4:n.186-437A>T | ||
| ENST00000647353.1:n.54-9151A>T | ||
| ENST00000651471.1:n.191-437A>T | ||
| ENST00000679909.1:c.28+14859A>T | ENSP00000506089.1:n.28+14859A>T | |
| ENST00000453660.3:n.168-437A>T | ||
| ENST00000538324.2:c.156-437A>T | ENSP00000483018.1:n.156-437A>T | |
| ENST00000611156.4:c.156-437A>T | ENSP00000483265.1:n.156-437A>T | |
| NM_020469.2:c.156-437A>T | NP_065202.2:n.156-437A>T | |
| NM_020469.3:c.156-437A>T | NP_065202.2:n.156-437A>T |