Linked Data
ClinVar Variation Id:
2116173
ClinVar RCV Id:
RCV003024588
dbSNP Id:
rs781321058
ExAC:
12:124156118 C / T
gnomAD v3:
12-123671571-C-T
gnomAD v4:
12-123671571-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.123671571C>T , CM000674.2:g.123671571C>T | GRCh38 |
| NC_000012.11:g.124156118C>T , CM000674.1:g.124156118C>T | GRCh37 |
| NC_000012.10:g.122722071C>T | NCBI36 |
| NG_030442.1:g.5459C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303372.7:c.147C>T MANE Select | ENSP00000304941.5:p.Thr49= | |
| ENST00000679504.1:c.147C>T | ENSP00000505006.1:p.Thr49= | |
| ENST00000680500.1:c.147C>T | ENSP00000506438.1:p.Thr49= | |
| ENST00000680574.1:c.147C>T | ENSP00000505356.1:p.Thr49= | |
| ENST00000303372.6:c.147C>T | ENSP00000304941.5:p.Thr49= | |
| ENST00000426174.6:c.147C>T | ENSP00000395171.2:p.Thr49= | |
| ENST00000541523.1:c.173C>T | ENSP00000437644.1:p.Pro58Leu | |
| NM_001143850.2:c.147C>T | NP_001137322.1:p.Thr49= | |
| NM_024809.4:c.147C>T | NP_079085.2:p.Thr49= | |
| XM_005253623.2:c.147C>T | XP_005253680.1:p.Thr49= | |
| XM_006719605.2:c.147C>T | XP_006719668.1:p.Thr49= | |
| XM_006719605.3:c.147C>T | XP_006719668.1:p.Thr49= | |
| XM_017019974.1:c.147C>T | XP_016875463.1:p.Thr49= | |
| XM_017019975.1:c.-636C>T | XP_016875464.1:n.-636C>T | |
| NM_024809.5:c.147C>T MANE Select | NP_079085.2:p.Thr49= | |
| NM_001143850.3:c.147C>T | NP_001137322.1:p.Thr49= |