Linked Data
MyVariant Identifiers:
chr9:g.136133510G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133258120G>T , CM000671.2:g.133258120G>T | GRCh38 |
| NC_000009.11:g.136133510G>T , CM000671.1:g.136133510G>T | GRCh37 |
| NC_000009.10:g.135123331G>T | NCBI36 |
| NG_006669.1:g.19544C>A | |
| NG_006669.2:g.22095C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000453660.4:n.246C>A | ||
| ENST00000647353.1:n.54-6968C>A | ||
| ENST00000651471.1:n.251C>A | ||
| ENST00000679909.1:c.28+17042C>A | ENSP00000506089.1:n.28+17042C>A | |
| ENST00000453660.3:n.228C>A | ||
| ENST00000538324.2:c.216C>A | ENSP00000483018.1:p.Pro72= | |
| ENST00000611156.4:c.216C>A | ENSP00000483265.1:p.Pro72= | |
| NM_020469.2:c.216C>A | NP_065202.2:p.Pro72= | |
| NM_020469.3:c.216C>A | NP_065202.2:p.Pro72= |