Linked Data
MyVariant Identifiers:
chr5:g.10286487T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.10286375T>G , CM000667.2:g.10286375T>G | GRCh38 |
| NC_000005.9:g.10286487T>G , CM000667.1:g.10286487T>G | GRCh37 |
| NC_000005.8:g.10339487T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296658.4:c.445A>C MANE Select | ENSP00000296658.3:p.Arg149= | |
| ENST00000296658.3:c.445A>C | ENSP00000296658.3:p.Arg149= | |
| ENST00000506821.1:n.699A>C | ||
| ENST00000510532.5:n.513A>C | ||
| ENST00000511963.5:n.553A>C | ||
| NM_138809.3:c.445A>C | NP_620164.1:p.Arg149= | |
| NM_138809.4:c.445A>C MANE Select | NP_620164.1:p.Arg149= |