MyVariant.info:
GRCh37
chr9:g.136132798C>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133257411C>T , CM000671.2:g.133257411C>T | GRCh38 |
| NC_000009.11:g.136132798C>T , CM000671.1:g.136132798C>T | GRCh37 |
| NC_000009.10:g.135122619C>T | NCBI36 |
| NG_006669.1:g.20257G>A | |
| NG_006669.2:g.22805G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.401G>A | ||
| ENST00000647353.1:n.54-6259G>A | ||
| ENST00000651471.1:n.329+631G>A | ||
| ENST00000679909.1:c.28+17751G>A | ENSP00000506089.1:n.28+17751G>A | |
| ENST00000453660.3:n.383G>A | ||
| ENST00000538324.2:c.369G>A | ENSP00000483018.1:p.Lys123= | |
| ENST00000611156.4:c.369G>A | ENSP00000483265.1:p.Lys123= | |
| NM_020469.2:c.372G>A | NP_065202.2:p.Lys124= | |
| NM_020469.3:c.372G>A | NP_065202.2:p.Lys124= |