Linked Data
MyVariant Identifiers:
chr5:g.158747339G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159320331G>A , CM000667.2:g.159320331G>A | GRCh38 |
| NC_000005.9:g.158747339G>A , CM000667.1:g.158747339G>A | GRCh37 |
| NC_000005.8:g.158679917G>A | NCBI36 |
| NG_009618.1:g.15143C>T , LRG_71:g.15143C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696750.1:c.42C>T | ENSP00000512849.1:p.Thr14= | |
| ENST00000696751.1:c.*167C>T | ENSP00000512850.1:n.*167C>T | |
| ENST00000231228.3:c.672C>T MANE Select | ENSP00000231228.2:p.Thr224= | |
| ENST00000231228.2:c.672C>T | ENSP00000231228.2:p.Thr224= | |
| NM_002187.2:c.672C>T , LRG_71t1:c.672C>T | NP_002178.2:p.Thr224= | |
| NM_002187.3:c.672C>T MANE Select | NP_002178.2:p.Thr224= |