Linked Data
ClinVar Variation Id:
1621293
dbSNP Id:
rs1428628208
MyVariant Identifiers:
chr12:g.58144501T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57750718T>G , CM000674.2:g.57750718T>G | GRCh38 |
| NC_000012.11:g.58144501T>G , CM000674.1:g.58144501T>G | GRCh37 |
| NC_000012.10:g.56430768T>G | NCBI36 |
| NG_007484.2:g.6664A>C , LRG_490:g.6664A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000257904.11:c.570A>C MANE Select | ENSP00000257904.5:p.Thr190= | |
| ENST00000257904.10:c.570A>C | ENSP00000257904.5:p.Thr190= | |
| ENST00000312990.10:c.265-47A>C | ENSP00000316889.6:n.265-47A>C | |
| ENST00000546489.5:c.348A>C | ENSP00000447779.1:p.Thr116= | |
| ENST00000547281.5:c.348A>C | ENSP00000447274.1:p.Thr116= | |
| ENST00000549606.5:c.-157-1214A>C | ENSP00000447005.1:n.-157-1214A>C | |
| ENST00000550419.5:c.523-155A>C | ENSP00000448098.1:n.523-155A>C | |
| ENST00000551800.5:c.348A>C | ENSP00000449391.1:p.Thr116= | |
| ENST00000551888.5:n.443-47A>C | ||
| ENST00000552254.5:c.570A>C | ENSP00000449179.1:p.Thr190= | |
| ENST00000553237.5:c.*209A>C | ENSP00000448885.1:n.*209A>C | |
| NM_000075.3:c.570A>C | NP_000066.1:p.Thr190= | |
| NM_000075.4:c.570A>C MANE Select | NP_000066.1:p.Thr190= |