Linked Data
MyVariant Identifiers:
chr9:g.136131092A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133255705A>T , CM000671.2:g.133255705A>T | GRCh38 |
| NC_000009.11:g.136131092A>T , CM000671.1:g.136131092A>T | GRCh37 |
| NC_000009.10:g.135120913A>T | NCBI36 |
| NG_006669.1:g.21963T>A | |
| NG_006669.2:g.24511T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000453660.4:n.1055T>A | ||
| ENST00000647353.1:n.54-4553T>A | ||
| ENST00000679909.1:c.28+19457T>A | ENSP00000506089.1:n.28+19457T>A | |
| ENST00000453660.3:n.1037T>A | ||
| ENST00000538324.2:c.1023T>A | ENSP00000483018.1:p.Thr341= | |
| ENST00000611156.4:c.1023T>A | ENSP00000483265.1:p.Thr341= | |
| NM_020469.2:c.1026T>A | NP_065202.2:p.Thr342= | |
| NM_020469.3:c.1026T>A | NP_065202.2:p.Thr342= |