Linked Data
MyVariant Identifiers:
chr1:g.24194522C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.23868032C>A , CM000663.2:g.23868032C>A | GRCh38 |
| NC_000001.10:g.24194522C>A , CM000663.1:g.24194522C>A | GRCh37 |
| NC_000001.9:g.24067109C>A | NCBI36 |
| NG_013346.1:g.5338G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374479.4:c.255G>T MANE Select | ENSP00000363603.3:p.Gly85= | |
| ENST00000374479.3:c.255G>T | ENSP00000363603.3:p.Gly85= | |
| NM_000147.4:c.255G>T | NP_000138.2:p.Gly85= | |
| XM_005245821.1:c.-295G>T | XP_005245878.1:n.-295G>T | |
| XM_005245821.3:c.-295G>T | XP_005245878.1:n.-295G>T | |
| NM_000147.5:c.255G>T MANE Select | NP_000138.2:p.Gly85= | |
| NR_174379.1:n.259G>T | ||
| NR_174380.1:n.259G>T | ||
| NR_174381.1:n.259G>T | ||
| NR_174382.1:n.259G>T |