Linked Data
MyVariant Identifiers:
chr8:g.19809288A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19951777A>T , CM000670.2:g.19951777A>T | GRCh38 |
| NC_000008.10:g.19809288A>T , CM000670.1:g.19809288A>T | GRCh37 |
| NC_000008.9:g.19853568A>T | NCBI36 |
| NG_008855.1:g.17707A>T | |
| NG_008855.2:g.55061A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.258A>T MANE Select | ENSP00000497642.1:p.Gly86= | |
| ENST00000311322.8:c.258A>T | ENSP00000309757.6:p.Gly86= | |
| ENST00000520959.5:c.30A>T | ENSP00000428496.1:p.Gly10= | |
| ENST00000521994.1:n.515A>T | ||
| ENST00000522701.5:c.258A>T | ENSP00000428557.1:p.Gly86= | |
| ENST00000524029.5:c.258A>T | ENSP00000428237.1:p.Gly86= | |
| NM_000237.2:c.258A>T | NP_000228.1:p.Gly86= | |
| NM_000237.3:c.258A>T MANE Select | NP_000228.1:p.Gly86= |