Linked Data
MyVariant Identifiers:
chr5:g.158747470T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159320462T>G , CM000667.2:g.159320462T>G | GRCh38 |
| NC_000005.9:g.158747470T>G , CM000667.1:g.158747470T>G | GRCh37 |
| NC_000005.8:g.158680048T>G | NCBI36 |
| NG_009618.1:g.15012A>C , LRG_71:g.15012A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696750.1:c.-90A>C | ENSP00000512849.1:n.-90A>C | |
| ENST00000696751.1:c.*36A>C | ENSP00000512850.1:n.*36A>C | |
| ENST00000231228.3:c.541A>C MANE Select | ENSP00000231228.2:p.Arg181= | |
| ENST00000231228.2:c.541A>C | ENSP00000231228.2:p.Arg181= | |
| NM_002187.2:c.541A>C , LRG_71t1:c.541A>C | NP_002178.2:p.Arg181= | |
| XR_001742945.1:n.13T>G | ||
| NM_002187.3:c.541A>C MANE Select | NP_002178.2:p.Arg181= |