Linked Data
MyVariant Identifiers:
chr1:g.94473794T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94008238T>A , CM000663.2:g.94008238T>A | GRCh38 |
| NC_000001.10:g.94473794T>A , CM000663.1:g.94473794T>A | GRCh37 |
| NC_000001.9:g.94246382T>A | NCBI36 |
| NG_009073.1:g.117912A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.5895A>T MANE Select | ENSP00000359245.3:p.Gly1965= | |
| ENST00000370225.3:c.5895A>T | ENSP00000359245.3:p.Gly1965= | |
| ENST00000465352.1:n.311A>T | ||
| ENST00000536513.5:c.2271A>T | ENSP00000439707.2:p.Gly757= | |
| NM_000350.2:c.5895A>T | NP_000341.2:p.Gly1965= | |
| NM_000350.3:c.5895A>T MANE Select | NP_000341.2:p.Gly1965= |