Linked Data
MyVariant Identifiers:
chr5:g.158747357G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159320349G>C , CM000667.2:g.159320349G>C | GRCh38 |
| NC_000005.9:g.158747357G>C , CM000667.1:g.158747357G>C | GRCh37 |
| NC_000005.8:g.158679935G>C | NCBI36 |
| NG_009618.1:g.15125C>G , LRG_71:g.15125C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696750.1:c.24C>G | ENSP00000512849.1:p.Leu8= | |
| ENST00000696751.1:c.*149C>G | ENSP00000512850.1:n.*149C>G | |
| ENST00000231228.3:c.654C>G MANE Select | ENSP00000231228.2:p.Leu218= | |
| ENST00000231228.2:c.654C>G | ENSP00000231228.2:p.Leu218= | |
| NM_002187.2:c.654C>G , LRG_71t1:c.654C>G | NP_002178.2:p.Leu218= | |
| NM_002187.3:c.654C>G MANE Select | NP_002178.2:p.Leu218= |