MyVariant.info:
GRCh37
chr9:g.136132813A>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133257426A>T , CM000671.2:g.133257426A>T | GRCh38 |
| NC_000009.11:g.136132813A>T , CM000671.1:g.136132813A>T | GRCh37 |
| NC_000009.10:g.135122634A>T | NCBI36 |
| NG_006669.1:g.20242T>A | |
| NG_006669.2:g.22790T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.386T>A | ||
| ENST00000647353.1:n.54-6274T>A | ||
| ENST00000651471.1:n.329+616T>A | ||
| ENST00000679909.1:c.28+17736T>A | ENSP00000506089.1:n.28+17736T>A | |
| ENST00000453660.3:n.368T>A | ||
| ENST00000538324.2:c.354T>A | ENSP00000483018.1:p.Thr118= | |
| ENST00000611156.4:c.354T>A | ENSP00000483265.1:p.Thr118= | |
| NM_020469.2:c.357T>A | NP_065202.2:p.Thr119= | |
| NM_020469.3:c.357T>A | NP_065202.2:p.Thr119= |