Linked Data
MyVariant Identifiers:
chr9:g.841931T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.841931T>C , CM000671.2:g.841931T>C | GRCh38 |
| NC_000009.11:g.841931T>C , CM000671.1:g.841931T>C | GRCh37 |
| NC_000009.10:g.831931T>C | NCBI36 |
| NG_009221.1:g.5242T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382276.8:c.93T>C MANE Select | ENSP00000371711.3:p.Phe31= | |
| ENST00000382276.7:c.93T>C | ENSP00000371711.3:p.Phe31= | |
| ENST00000564322.1:n.242T>C | ||
| NM_021951.2:c.93T>C | NP_068770.2:p.Phe31= | |
| XM_006716732.1:c.93T>C | XP_006716795.1:p.Phe31= | |
| XM_017014375.1:c.93T>C | XP_016869864.1:p.Phe31= | |
| NM_021951.3:c.93T>C MANE Select | NP_068770.2:p.Phe31= |