Linked Data
gnomAD v4:
9-133261495-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133261495C>A , CM000671.2:g.133261495C>A | GRCh38 |
| NC_000009.11:g.136136898C>A , CM000671.1:g.136136898C>A | GRCh37 |
| NC_000009.10:g.135126719C>A | NCBI36 |
| NG_006669.1:g.16155G>T | |
| NG_006669.2:g.18720G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.129-121G>T | ||
| ENST00000647353.1:n.54-10343G>T | ||
| ENST00000651471.1:n.134-121G>T | ||
| ENST00000679909.1:c.28+13667G>T | ENSP00000506089.1:n.28+13667G>T | |
| ENST00000453660.3:n.111-121G>T | ||
| ENST00000538324.2:c.99-121G>T | ENSP00000483018.1:n.99-121G>T | |
| ENST00000611156.4:c.99-121G>T | ENSP00000483265.1:n.99-121G>T | |
| NM_020469.2:c.99-121G>T | NP_065202.2:n.99-121G>T | |
| NM_020469.3:c.99-121G>T | NP_065202.2:n.99-121G>T |