Linked Data
MyVariant Identifiers:
chr8:g.37823715C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37966197C>T , CM000670.2:g.37966197C>T | GRCh38 |
| NC_000008.10:g.37823715C>T , CM000670.1:g.37823715C>T | GRCh37 |
| NC_000008.9:g.37942872C>T | NCBI36 |
| NG_011936.1:g.5470G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000345060.5:c.273G>A MANE Select | ENSP00000343782.3:p.Val91= | |
| ENST00000520341.2:n.401G>A | ||
| ENST00000345060.4:c.273G>A | ENSP00000343782.3:p.Val91= | |
| ENST00000614635.1:c.273G>A | ENSP00000480325.1:p.Val91= | |
| NM_000025.2:c.273G>A | NP_000016.1:p.Val91= | |
| NM_000025.3:c.273G>A MANE Select | NP_000016.1:p.Val91= |