Linked Data
gnomAD v4:
22-36564741-C-T
COSMIC:
COSM3964252
MyVariant Identifiers:
chr22:g.36960788C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.36564741C>T , CM000684.2:g.36564741C>T | GRCh38 |
| NC_000022.10:g.36960788C>T , CM000684.1:g.36960788C>T | GRCh37 |
| NC_000022.9:g.35290734C>T | NCBI36 |
| NG_031861.1:g.142903G>A | |
| NG_031861.2:g.143118G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300105.7:c.582G>A MANE Select | ENSP00000300105.6:p.Gly194= | |
| ENST00000300105.6:c.582G>A | ENSP00000300105.6:p.Gly194= | |
| NM_006078.3:c.582G>A | NP_006069.1:p.Gly194= | |
| NM_006078.4:c.582G>A | NP_006069.1:p.Gly194= | |
| XM_017028531.2:c.324G>A | XP_016884020.1:p.Gly108= | |
| NM_001379051.1:c.513G>A | NP_001365980.1:p.Gly171= | |
| NM_006078.5:c.582G>A MANE Select | NP_006069.1:p.Gly194= | |
| NR_166440.1:n.1948G>A |