Linked Data
MyVariant Identifiers:
chr8:g.19811644T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19954133T>G , CM000670.2:g.19954133T>G | GRCh38 |
| NC_000008.10:g.19811644T>G , CM000670.1:g.19811644T>G | GRCh37 |
| NC_000008.9:g.19855924T>G | NCBI36 |
| NG_008855.1:g.20063T>G | |
| NG_008855.2:g.57417T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000650287.1:c.555T>G MANE Select | ENSP00000497642.1:p.Ala185= | |
| ENST00000311322.8:c.555T>G | ENSP00000309757.6:p.Ala185= | |
| ENST00000520959.5:c.327T>G | ENSP00000428496.1:p.Ala109= | |
| NM_000237.2:c.555T>G | NP_000228.1:p.Ala185= | |
| NM_000237.3:c.555T>G MANE Select | NP_000228.1:p.Ala185= |