Linked Data
MyVariant Identifiers:
chr1:g.169499036G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169529798G>T , CM000663.2:g.169529798G>T | GRCh38 |
| NC_000001.10:g.169499036G>T , CM000663.1:g.169499036G>T | GRCh37 |
| NC_000001.9:g.167765660G>T | NCBI36 |
| NG_011806.1:g.61734C>A , LRG_553:g.61734C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367797.9:c.5229C>A MANE Select | ENSP00000356771.3:p.Gly1743= | |
| ENST00000367796.3:c.5244C>A | ENSP00000356770.3:p.Gly1748= | |
| ENST00000367797.7:c.5229C>A | ENSP00000356771.3:p.Gly1743= | |
| NM_000130.4:c.5229C>A , LRG_553t1:c.5229C>A | NP_000121.2:p.Gly1743= | |
| XM_017000660.2:c.4818C>A | XP_016856149.1:p.Gly1606= | |
| NM_000130.5:c.5229C>A MANE Select | NP_000121.2:p.Gly1743= |