Linked Data
MyVariant Identifiers:
chr12:g.111351061C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.110913257C>G , CM000674.2:g.110913257C>G | GRCh38 |
| NC_000012.11:g.111351061C>G , CM000674.1:g.111351061C>G | GRCh37 |
| NC_000012.10:g.109835444C>G | NCBI36 |
| NG_007554.1:g.12321G>C , LRG_393:g.12321G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000228841.15:c.342G>C MANE Select | ENSP00000228841.8:p.Leu114= | |
| ENST00000663220.1:c.285G>C | ENSP00000499568.1:p.Leu95= | |
| ENST00000228841.12:c.342G>C | ENSP00000228841.7:p.Leu114= | |
| ENST00000548438.1:c.300G>C | ENSP00000447154.1:p.Leu100= | |
| ENST00000549029.1:n.173G>C | ||
| NM_000432.3:c.342G>C , LRG_393t1:c.342G>C | NP_000423.2:p.Leu114= | |
| NM_000432.4:c.342G>C MANE Select | NP_000423.2:p.Leu114= |