Linked Data
MyVariant Identifiers:
chr5:g.158747411T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159320403T>G , CM000667.2:g.159320403T>G | GRCh38 |
| NC_000005.9:g.158747411T>G , CM000667.1:g.158747411T>G | GRCh37 |
| NC_000005.8:g.158679989T>G | NCBI36 |
| NG_009618.1:g.15071A>C , LRG_71:g.15071A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696750.1:c.-31A>C | ENSP00000512849.1:n.-31A>C | |
| ENST00000696751.1:c.*95A>C | ENSP00000512850.1:n.*95A>C | |
| ENST00000231228.3:c.600A>C MANE Select | ENSP00000231228.2:p.Pro200= | |
| ENST00000231228.2:c.600A>C | ENSP00000231228.2:p.Pro200= | |
| NM_002187.2:c.600A>C , LRG_71t1:c.600A>C | NP_002178.2:p.Pro200= | |
| NM_002187.3:c.600A>C MANE Select | NP_002178.2:p.Pro200= |