Linked Data
MyVariant Identifiers:
chr22:g.36960932A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.36564885A>T , CM000684.2:g.36564885A>T | GRCh38 |
| NC_000022.10:g.36960932A>T , CM000684.1:g.36960932A>T | GRCh37 |
| NC_000022.9:g.35290878A>T | NCBI36 |
| NG_031861.1:g.142759T>A | |
| NG_031861.2:g.142974T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300105.7:c.438T>A MANE Select | ENSP00000300105.6:p.Gly146= | |
| ENST00000300105.6:c.438T>A | ENSP00000300105.6:p.Gly146= | |
| NM_006078.3:c.438T>A | NP_006069.1:p.Gly146= | |
| NM_006078.4:c.438T>A | NP_006069.1:p.Gly146= | |
| XM_017028531.2:c.180T>A | XP_016884020.1:p.Gly60= | |
| NM_001379051.1:c.369T>A | NP_001365980.1:p.Gly123= | |
| NM_006078.5:c.438T>A MANE Select | NP_006069.1:p.Gly146= | |
| NR_166440.1:n.1804T>A |