Linked Data
MyVariant Identifiers:
chr9:g.136132828G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133257441G>T , CM000671.2:g.133257441G>T | GRCh38 |
| NC_000009.11:g.136132828G>T , CM000671.1:g.136132828G>T | GRCh37 |
| NC_000009.10:g.135122649G>T | NCBI36 |
| NG_006669.1:g.20227C>A | |
| NG_006669.2:g.22775C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.371C>A | ||
| ENST00000647353.1:n.54-6289C>A | ||
| ENST00000651471.1:n.329+601C>A | ||
| ENST00000679909.1:c.28+17721C>A | ENSP00000506089.1:n.28+17721C>A | |
| ENST00000453660.3:n.353C>A | ||
| ENST00000538324.2:c.339C>A | ENSP00000483018.1:p.Thr113= | |
| ENST00000611156.4:c.339C>A | ENSP00000483265.1:p.Thr113= | |
| NM_020469.2:c.342C>A | NP_065202.2:p.Thr114= | |
| NM_020469.3:c.342C>A | NP_065202.2:p.Thr114= |