Linked Data
MyVariant Identifiers:
chr9:g.136131686G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133256299G>T , CM000671.2:g.133256299G>T | GRCh38 |
| NC_000009.11:g.136131686G>T , CM000671.1:g.136131686G>T | GRCh37 |
| NC_000009.10:g.135121507G>T | NCBI36 |
| NG_006669.1:g.21369C>A | |
| NG_006669.2:g.23917C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.461C>A | ||
| ENST00000647353.1:n.54-5147C>A | ||
| ENST00000651471.1:n.387C>A | ||
| ENST00000679909.1:c.28+18863C>A | ENSP00000506089.1:n.28+18863C>A | |
| ENST00000453660.3:n.443C>A | ||
| ENST00000538324.2:c.429C>A | ENSP00000483018.1:p.Gly143= | |
| ENST00000611156.4:c.429C>A | ENSP00000483265.1:p.Gly143= | |
| NM_020469.2:c.432C>A | NP_065202.2:p.Gly144= | |
| NM_020469.3:c.432C>A | NP_065202.2:p.Gly144= |