Linked Data
MyVariant Identifiers:
chr19:g.41354214C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.40848309C>G , CM000681.2:g.40848309C>G | GRCh38 |
| NC_000019.9:g.41354214C>G , CM000681.1:g.41354214C>G | GRCh37 |
| NC_000019.8:g.46046054C>G | NCBI36 |
| NG_008377.1:g.7139G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301141.10:c.564G>C MANE Select | ENSP00000301141.4:p.Gly188= | |
| ENST00000301141.9:c.564G>C | ENSP00000301141.4:p.Gly188= | |
| ENST00000596719.5:n.415G>C | ||
| ENST00000600495.1:c.*376G>C | ENSP00000472905.1:n.*376G>C | |
| ENST00000601627.1:c.120-43682C>G | ||
| ENST00000610301.1:c.564G>C | ENSP00000477899.1:p.Gly188= | |
| NM_000762.5:c.564G>C | NP_000753.3:p.Gly188= | |
| NM_000762.6:c.564G>C MANE Select | NP_000753.3:p.Gly188= |