Linked Data
MyVariant Identifiers:
chr9:g.136131665G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133256278G>T , CM000671.2:g.133256278G>T | GRCh38 |
| NC_000009.11:g.136131665G>T , CM000671.1:g.136131665G>T | GRCh37 |
| NC_000009.10:g.135121486G>T | NCBI36 |
| NG_006669.1:g.21390C>A | |
| NG_006669.2:g.23938C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000453660.4:n.482C>A | ||
| ENST00000647353.1:n.54-5126C>A | ||
| ENST00000651471.1:n.408C>A | ||
| ENST00000679909.1:c.28+18884C>A | ENSP00000506089.1:n.28+18884C>A | |
| ENST00000453660.3:n.464C>A | ||
| ENST00000538324.2:c.450C>A | ENSP00000483018.1:p.Val150= | |
| ENST00000611156.4:c.450C>A | ENSP00000483265.1:p.Val150= | |
| NM_020469.2:c.453C>A | NP_065202.2:p.Val151= | |
| NM_020469.3:c.453C>A | NP_065202.2:p.Val151= |