Linked Data
gnomAD v4:
9-133258030-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133258030G>T , CM000671.2:g.133258030G>T | GRCh38 |
| NC_000009.11:g.136133420G>T , CM000671.1:g.136133420G>T | GRCh37 |
| NC_000009.10:g.135123241G>T | NCBI36 |
| NG_006669.1:g.19634C>A | |
| NG_006669.2:g.22185C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.269+67C>A | ||
| ENST00000647353.1:n.54-6878C>A | ||
| ENST00000651471.1:n.329+12C>A | ||
| ENST00000679909.1:c.28+17132C>A | ENSP00000506089.1:n.28+17132C>A | |
| ENST00000453660.3:n.251+67C>A | ||
| ENST00000538324.2:c.239+67C>A | ENSP00000483018.1:n.239+67C>A | |
| ENST00000611156.4:c.239+67C>A | ENSP00000483265.1:n.239+67C>A | |
| NM_020469.2:c.239+67C>A | NP_065202.2:n.239+67C>A | |
| NM_020469.3:c.239+67C>A | NP_065202.2:n.239+67C>A |