Linked Data
MyVariant Identifiers:
chr14:g.37132331C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.36663126C>G , CM000676.2:g.36663126C>G | GRCh38 |
| NC_000014.8:g.37132331C>G , CM000676.1:g.37132331C>G | GRCh37 |
| NC_000014.7:g.36202082C>G | NCBI36 |
| NG_013357.1:g.10559C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361487.7:c.234C>G MANE Select | ENSP00000355245.6:p.Val78= | |
| ENST00000555639.2:c.234C>G | ENSP00000501203.1:p.Val78= | |
| ENST00000361487.6:c.234C>G | ENSP00000355245.6:p.Val78= | |
| ENST00000402703.6:c.234C>G | ENSP00000384817.2:p.Val78= | |
| ENST00000554201.1:c.-328C>G | ENSP00000450434.1:n.-328C>G | |
| ENST00000555639.1:n.536C>G | ||
| NM_006194.3:c.234C>G | NP_006185.1:p.Val78= | |
| NM_001372076.1:c.234C>G MANE Select | NP_001359005.1:p.Val78= | |
| NM_006194.4:c.234C>G | NP_006185.1:p.Val78= |