Linked Data
MyVariant Identifiers:
chr9:g.101304176T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.98541894T>C , CM000671.2:g.98541894T>C | GRCh38 |
| NC_000009.11:g.101304176T>C , CM000671.1:g.101304176T>C | GRCh37 |
| NC_000009.10:g.100343997T>C | NCBI36 |
| NG_016426.1:g.172304A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259455.4:c.609A>G MANE Select | ENSP00000259455.2:p.Gln203= | |
| ENST00000637410.1:n.387A>G | ||
| ENST00000637717.1:c.225A>G | ENSP00000490789.1:p.Gln75= | |
| ENST00000259455.3:c.609A>G | ENSP00000259455.2:p.Gln203= | |
| ENST00000477471.1:n.396A>G | ||
| ENST00000634227.1:n.383A>G | ||
| NM_005458.7:c.609A>G | NP_005449.5:p.Gln203= | |
| XM_017015331.2:c.315A>G | XP_016870820.1:p.Gln105= | |
| NM_005458.8:c.609A>G MANE Select | NP_005449.5:p.Gln203= |