Linked Data
MyVariant Identifiers:
chr9:g.136131662G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133256275G>A , CM000671.2:g.133256275G>A | GRCh38 |
| NC_000009.11:g.136131662G>A , CM000671.1:g.136131662G>A | GRCh37 |
| NC_000009.10:g.135121483G>A | NCBI36 |
| NG_006669.1:g.21393C>T | |
| NG_006669.2:g.23941C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000453660.4:n.485C>T | ||
| ENST00000647353.1:n.54-5123C>T | ||
| ENST00000651471.1:n.411C>T | ||
| ENST00000679909.1:c.28+18887C>T | ENSP00000506089.1:n.28+18887C>T | |
| ENST00000453660.3:n.467C>T | ||
| ENST00000538324.2:c.453C>T | ENSP00000483018.1:p.Phe151= | |
| ENST00000611156.4:c.453C>T | ENSP00000483265.1:p.Phe151= | |
| NM_020469.2:c.456C>T | NP_065202.2:p.Phe152= | |
| NM_020469.3:c.456C>T | NP_065202.2:p.Phe152= |