Linked Data
MyVariant Identifiers:
chr1:g.116275522C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115732901C>A , CM000663.2:g.115732901C>A | GRCh38 |
| NC_000001.10:g.116275522C>A , CM000663.1:g.116275522C>A | GRCh37 |
| NC_000001.9:g.116077045C>A | NCBI36 |
| NG_008802.1:g.40905G>T , LRG_404:g.40905G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000488931.2:c.330G>T | ENSP00000518226.1:p.Gly110= | |
| ENST00000261448.6:c.606G>T MANE Select | ENSP00000261448.5:p.Gly202= | |
| ENST00000261448.5:c.606G>T | ENSP00000261448.5:p.Gly202= | |
| ENST00000488931.1:n.27G>T | ||
| NM_001232.3:c.606G>T , LRG_404t1:c.606G>T | NP_001223.2:p.Gly202= | |
| NM_001232.4:c.606G>T MANE Select | NP_001223.2:p.Gly202= |