Linked Data
ClinVar Variation Id:
3006563
ClinVar RCV Id:
RCV003861178
MyVariant Identifiers:
chr12:g.48238643C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.47844860C>T , CM000674.2:g.47844860C>T | GRCh38 |
| NC_000012.11:g.48238643C>T , CM000674.1:g.48238643C>T | GRCh37 |
| NC_000012.10:g.46524910C>T | NCBI36 |
| NG_008731.1:g.65172G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229022.9:c.1170G>A | ENSP00000229022.5:p.Leu390= | |
| ENST00000549336.6:c.1170G>A MANE Select | ENSP00000449573.2:p.Leu390= | |
| ENST00000229022.7:c.1170G>A | ENSP00000229022.3:p.Leu390= | |
| ENST00000395324.6:c.1170G>A | ENSP00000378734.2:p.Leu390= | |
| ENST00000547065.1:c.*1172G>A | ENSP00000449074.1:n.*1172G>A | |
| ENST00000549336.5:c.1170G>A | ENSP00000449573.1:p.Leu390= | |
| ENST00000550325.5:c.1320G>A | ENSP00000447173.1:p.Leu440= | |
| NM_000376.2:c.1170G>A | NP_000367.1:p.Leu390= | |
| NM_001017535.1:c.1170G>A | NP_001017535.1:p.Leu390= | |
| NM_001017536.1:c.1320G>A | NP_001017536.1:p.Leu440= | |
| XM_006719587.2:c.1170G>A | XP_006719650.1:p.Leu390= | |
| XM_011538720.1:c.1170G>A | XP_011537022.1:p.Leu390= | |
| NM_001364085.1:c.1170G>A | NP_001351014.1:p.Leu390= | |
| XM_006719587.3:c.1170G>A | XP_006719650.1:p.Leu390= | |
| XM_011538720.2:c.1170G>A | XP_011537022.1:p.Leu390= | |
| XM_024449178.1:c.1239G>A | XP_024304946.1:p.Leu413= | |
| NM_000376.3:c.1170G>A MANE Select | NP_000367.1:p.Leu390= | |
| NM_001017535.2:c.1170G>A | NP_001017535.1:p.Leu390= | |
| NM_001017536.2:c.1320G>A | NP_001017536.1:p.Leu440= | |
| NM_001364085.2:c.1170G>A | NP_001351014.1:p.Leu390= | |
| NM_001374661.1:c.1170G>A | NP_001361590.1:p.Leu390= | |
| NM_001374662.1:c.1170G>A | NP_001361591.1:p.Leu390= |