Linked Data
MyVariant Identifiers:
chr1:g.24194564G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.23868074G>T , CM000663.2:g.23868074G>T | GRCh38 |
| NC_000001.10:g.24194564G>T , CM000663.1:g.24194564G>T | GRCh37 |
| NC_000001.9:g.24067151G>T | NCBI36 |
| NG_013346.1:g.5296C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374479.4:c.213C>A MANE Select | ENSP00000363603.3:p.Ala71= | |
| ENST00000374479.3:c.213C>A | ENSP00000363603.3:p.Ala71= | |
| NM_000147.4:c.213C>A | NP_000138.2:p.Ala71= | |
| XM_005245821.1:c.-337C>A | XP_005245878.1:n.-337C>A | |
| XM_005245821.3:c.-337C>A | XP_005245878.1:n.-337C>A | |
| NM_000147.5:c.213C>A MANE Select | NP_000138.2:p.Ala71= | |
| NR_174379.1:n.217C>A | ||
| NR_174380.1:n.217C>A | ||
| NR_174381.1:n.217C>A | ||
| NR_174382.1:n.217C>A |