Linked Data
gnomAD v4:
1-23867926-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.23867926C>T , CM000663.2:g.23867926C>T | GRCh38 |
| NC_000001.10:g.24194416C>T , CM000663.1:g.24194416C>T | GRCh37 |
| NC_000001.9:g.24067003C>T | NCBI36 |
| NG_013346.1:g.5444G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374479.4:c.361G>A MANE Select | ENSP00000363603.3:p.Ala121Thr | |
| ENST00000374479.3:c.361G>A | ENSP00000363603.3:p.Ala121Thr | |
| NM_000147.4:c.361G>A | NP_000138.2:p.Ala121Thr | |
| XM_005245821.1:c.-189G>A | XP_005245878.1:n.-189G>A | |
| XM_005245821.3:c.-189G>A | XP_005245878.1:n.-189G>A | |
| NM_000147.5:c.361G>A MANE Select | NP_000138.2:p.Ala121Thr | |
| NR_174379.1:n.365G>A | ||
| NR_174380.1:n.365G>A | ||
| NR_174381.1:n.365G>A | ||
| NR_174382.1:n.365G>A |