Linked Data
MyVariant Identifiers:
chr9:g.136131188C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133255801C>A , CM000671.2:g.133255801C>A | GRCh38 |
| NC_000009.11:g.136131188C>A , CM000671.1:g.136131188C>A | GRCh37 |
| NC_000009.10:g.135121009C>A | NCBI36 |
| NG_006669.1:g.21867G>T | |
| NG_006669.2:g.24415G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000453660.4:n.959G>T | ||
| ENST00000647353.1:n.54-4649G>T | ||
| ENST00000679909.1:c.28+19361G>T | ENSP00000506089.1:n.28+19361G>T | |
| ENST00000453660.3:n.941G>T | ||
| ENST00000538324.2:c.927G>T | ENSP00000483018.1:p.Leu309= | |
| ENST00000611156.4:c.927G>T | ENSP00000483265.1:p.Leu309= | |
| NM_020469.2:c.930G>T | NP_065202.2:p.Leu310= | |
| NM_020469.3:c.930G>T | NP_065202.2:p.Leu310= |