Linked Data
MyVariant Identifiers:
chr9:g.101340232G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.98577950G>C , CM000671.2:g.98577950G>C | GRCh38 |
| NC_000009.11:g.101340232G>C , CM000671.1:g.101340232G>C | GRCh37 |
| NC_000009.10:g.100380053G>C | NCBI36 |
| NG_016426.1:g.136248C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259455.4:c.444C>G MANE Select | ENSP00000259455.2:p.Gly148= | |
| ENST00000637410.1:n.222C>G | ||
| ENST00000637717.1:c.60C>G | ENSP00000490789.1:p.Gly20= | |
| ENST00000259455.3:c.444C>G | ENSP00000259455.2:p.Gly148= | |
| ENST00000634227.1:n.218C>G | ||
| NM_005458.7:c.444C>G | NP_005449.5:p.Gly148= | |
| NM_005458.8:c.444C>G MANE Select | NP_005449.5:p.Gly148= |