Linked Data
MyVariant Identifiers:
chr2:g.233406231T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232541521T>G , CM000664.2:g.232541521T>G | GRCh38 |
| NC_000002.11:g.233406231T>G , CM000664.1:g.233406231T>G | GRCh37 |
| NC_000002.10:g.233114475T>G | NCBI36 |
| NG_012954.1:g.6795T>G | |
| NG_012954.2:g.6830T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651502.1:c.498T>G MANE Select | ENSP00000498757.1:p.Leu166= | |
| ENST00000389492.3:c.350+810T>G | ENSP00000374143.3:n.350+810T>G | |
| ENST00000389494.7:c.498T>G | ENSP00000374145.3:p.Leu166= | |
| ENST00000485094.1:n.519T>G | ||
| NM_005199.4:c.498T>G | NP_005190.4:p.Leu166= | |
| NM_005199.5:c.498T>G MANE Select | NP_005190.4:p.Leu166= |