Linked Data
MyVariant Identifiers:
chr9:g.136130833G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133255446G>C , CM000671.2:g.133255446G>C | GRCh38 |
| NC_000009.11:g.136130833G>C , CM000671.1:g.136130833G>C | GRCh37 |
| NC_000009.10:g.135120654G>C | NCBI36 |
| NG_006669.1:g.22222C>G | |
| NG_006669.2:g.24770C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.1314C>G | ||
| ENST00000647353.1:n.54-4294C>G | ||
| ENST00000679909.1:c.28+19716C>G | ENSP00000506089.1:n.28+19716C>G | |
| ENST00000453660.3:n.1296C>G | ||
| ENST00000611156.4:c.*220C>G | ENSP00000483265.1:n.*220C>G | |
| NM_020469.2:c.*220C>G | NP_065202.2:n.*220C>G | |
| NM_020469.3:c.*220C>G | NP_065202.2:n.*220C>G |