Linked Data
MyVariant Identifiers:
chr9:g.101304299A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.98542017A>T , CM000671.2:g.98542017A>T | GRCh38 |
| NC_000009.11:g.101304299A>T , CM000671.1:g.101304299A>T | GRCh37 |
| NC_000009.10:g.100344120A>T | NCBI36 |
| NG_016426.1:g.172181T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259455.4:c.486T>A MANE Select | ENSP00000259455.2:p.Val162= | |
| ENST00000637410.1:n.264T>A | ||
| ENST00000637717.1:c.102T>A | ENSP00000490789.1:p.Val34= | |
| ENST00000638001.1:n.96T>A | ||
| ENST00000259455.3:c.486T>A | ENSP00000259455.2:p.Val162= | |
| ENST00000477471.1:n.273T>A | ||
| ENST00000634227.1:n.260T>A | ||
| NM_005458.7:c.486T>A | NP_005449.5:p.Val162= | |
| XM_017015331.2:c.192T>A | XP_016870820.1:p.Val64= | |
| NM_005458.8:c.486T>A MANE Select | NP_005449.5:p.Val162= |