Linked Data
gnomAD v4:
9-133258017-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133258017C>T , CM000671.2:g.133258017C>T | GRCh38 |
| NC_000009.11:g.136133407C>T , CM000671.1:g.136133407C>T | GRCh37 |
| NC_000009.10:g.135123228C>T | NCBI36 |
| NG_006669.1:g.19647G>A | |
| NG_006669.2:g.22198G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000453660.4:n.269+80G>A | ||
| ENST00000647353.1:n.54-6865G>A | ||
| ENST00000651471.1:n.329+25G>A | ||
| ENST00000679909.1:c.28+17145G>A | ENSP00000506089.1:n.28+17145G>A | |
| ENST00000453660.3:n.251+80G>A | ||
| ENST00000538324.2:c.239+80G>A | ENSP00000483018.1:n.239+80G>A | |
| ENST00000611156.4:c.239+80G>A | ENSP00000483265.1:n.239+80G>A | |
| NM_020469.2:c.239+80G>A | NP_065202.2:n.239+80G>A | |
| NM_020469.3:c.239+80G>A | NP_065202.2:n.239+80G>A |