Linked Data
dbSNP Id:
rs1566152942
gnomAD v4:
12-109595108-C-T
MyVariant Identifiers:
chr12:g.110032913C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.109595108C>T , CM000674.2:g.109595108C>T | GRCh38 |
| NC_000012.11:g.110032913C>T , CM000674.1:g.110032913C>T | GRCh37 |
| NC_000012.10:g.108517296C>T | NCBI36 |
| NG_007702.1:g.26414C>T , LRG_156:g.26414C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000539696.6:c.123C>T | ENSP00000439134.1:p.Thr41= | |
| ENST00000546277.6:c.966C>T | ENSP00000438153.2:p.Thr322= | |
| ENST00000636529.2:n.605C>T | ||
| ENST00000697195.1:c.*730C>T | ENSP00000513181.1:n.*730C>T | |
| ENST00000697196.1:c.*139C>T | ENSP00000513182.1:n.*139C>T | |
| ENST00000697197.1:n.2995C>T | ||
| ENST00000697198.1:n.1350C>T | ||
| ENST00000228510.8:c.966C>T MANE Select | ENSP00000228510.3:p.Thr322= | |
| ENST00000636529.1:c.591C>T | ||
| ENST00000636996.1:c.814C>T | ||
| ENST00000228510.7:c.966C>T | ENSP00000228510.3:p.Thr322= | |
| ENST00000392727.7:c.810C>T | ENSP00000376487.3:p.Thr270= | |
| ENST00000447878.6:c.*413C>T | ENSP00000415555.2:n.*413C>T | |
| ENST00000537237.5:c.*639C>T | ENSP00000445382.1:n.*639C>T | |
| ENST00000539575.4:c.966C>T | ENSP00000443551.2:p.Thr322= | |
| ENST00000539696.5:c.123C>T | ENSP00000439134.1:p.Thr41= | |
| ENST00000540353.1:n.3199C>T | ||
| ENST00000625889.2:c.810C>T | ENSP00000486846.1:p.Thr270= | |
| ENST00000629016.2:c.*413C>T | ENSP00000486804.1:n.*413C>T | |
| NM_000431.3:c.966C>T | NP_000422.1:p.Thr322= | |
| NM_001114185.2:c.966C>T | NP_001107657.1:p.Thr322= | |
| NM_001301182.1:c.810C>T | NP_001288111.1:p.Thr270= | |
| XM_011538372.1:c.966C>T | XP_011536674.1:p.Thr322= | |
| XM_017019313.2:c.810C>T | XP_016874802.1:p.Thr270= | |
| XM_017019314.1:c.966C>T | XP_016874803.1:p.Thr322= | |
| NM_000431.4:c.966C>T MANE Select | NP_000422.1:p.Thr322= | |
| NM_001114185.3:c.966C>T | NP_001107657.1:p.Thr322= | |
| NM_001301182.2:c.810C>T | NP_001288111.1:p.Thr270= |