Linked Data
MyVariant Identifiers:
chr1:g.116275585A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115732964A>T , CM000663.2:g.115732964A>T | GRCh38 |
| NC_000001.10:g.116275585A>T , CM000663.1:g.116275585A>T | GRCh37 |
| NC_000001.9:g.116077108A>T | NCBI36 |
| NG_008802.1:g.40842T>A , LRG_404:g.40842T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000488931.2:c.267T>A | ENSP00000518226.1:p.Ala89= | |
| ENST00000261448.6:c.543T>A MANE Select | ENSP00000261448.5:p.Ala181= | |
| ENST00000261448.5:c.543T>A | ENSP00000261448.5:p.Ala181= | |
| NM_001232.3:c.543T>A , LRG_404t1:c.543T>A | NP_001223.2:p.Ala181= | |
| NM_001232.4:c.543T>A MANE Select | NP_001223.2:p.Ala181= |