Linked Data
MyVariant Identifiers:
chr10:g.104597047A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102837290A>T , CM000672.2:g.102837290A>T | GRCh38 |
| NC_000010.10:g.104597047A>T , CM000672.1:g.104597047A>T | GRCh37 |
| NC_000010.9:g.104587037A>T | NCBI36 |
| NG_007955.1:g.5244T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000369887.4:c.72T>A MANE Select | ENSP00000358903.3:p.Gly24= | |
| ENST00000638190.1:c.72T>A | ENSP00000492539.1:p.Gly24= | |
| ENST00000638272.1:c.72T>A | ENSP00000491508.1:p.Gly24= | |
| ENST00000638971.1:c.72T>A | ENSP00000492313.1:p.Gly24= | |
| ENST00000639393.1:c.72T>A | ENSP00000492651.1:p.Gly24= | |
| ENST00000369887.3:c.72T>A | ENSP00000358903.3:p.Gly24= | |
| ENST00000489268.1:n.125T>A | ||
| NM_000102.3:c.72T>A | NP_000093.1:p.Gly24= | |
| NM_000102.4:c.72T>A MANE Select | NP_000093.1:p.Gly24= |