Linked Data
MyVariant Identifiers:
chr1:g.116275591G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115732970G>A , CM000663.2:g.115732970G>A | GRCh38 |
| NC_000001.10:g.116275591G>A , CM000663.1:g.116275591G>A | GRCh37 |
| NC_000001.9:g.116077114G>A | NCBI36 |
| NG_008802.1:g.40836C>T , LRG_404:g.40836C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000488931.2:c.261C>T | ENSP00000518226.1:p.Tyr87= | |
| ENST00000261448.6:c.537C>T MANE Select | ENSP00000261448.5:p.Tyr179= | |
| ENST00000261448.5:c.537C>T | ENSP00000261448.5:p.Tyr179= | |
| NM_001232.3:c.537C>T , LRG_404t1:c.537C>T | NP_001223.2:p.Tyr179= | |
| NM_001232.4:c.537C>T MANE Select | NP_001223.2:p.Tyr179= |