Linked Data
MyVariant Identifiers:
chr12:g.111352081C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.110914277C>A , CM000674.2:g.110914277C>A | GRCh38 |
| NC_000012.11:g.111352081C>A , CM000674.1:g.111352081C>A | GRCh37 |
| NC_000012.10:g.109836464C>A | NCBI36 |
| NG_007554.1:g.11301G>T , LRG_393:g.11301G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000228841.15:c.183G>T MANE Select | ENSP00000228841.8:p.Val61= | |
| ENST00000663220.1:c.126G>T | ENSP00000499568.1:p.Val42= | |
| ENST00000228841.12:c.183G>T | ENSP00000228841.7:p.Val61= | |
| ENST00000548438.1:c.141G>T | ENSP00000447154.1:p.Val47= | |
| ENST00000549029.1:n.14G>T | ||
| NM_000432.3:c.183G>T , LRG_393t1:c.183G>T | NP_000423.2:p.Val61= | |
| NM_000432.4:c.183G>T MANE Select | NP_000423.2:p.Val61= |