Linked Data
MyVariant Identifiers:
chr17:g.37822248C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39665995C>A , CM000679.2:g.39665995C>A | GRCh38 |
| NC_000017.10:g.37822248C>A , CM000679.1:g.37822248C>A | GRCh37 |
| NC_000017.9:g.35075774C>A | NCBI36 |
| NG_008892.1:g.5650C>A , LRG_210:g.5650C>A | |
| NG_042278.1:g.3015C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309889.3:c.390C>A MANE Select | ENSP00000312624.2:p.Arg130= | |
| ENST00000309889.2:c.390C>A | ENSP00000312624.2:p.Arg130= | |
| ENST00000578283.1:c.318C>A | ENSP00000462787.1:p.Arg106= | |
| NM_003673.3:c.390C>A , LRG_210t1:c.390C>A | NP_003664.1:p.Arg130= | |
| NM_003673.4:c.390C>A MANE Select | NP_003664.1:p.Arg130= |