Linked Data
ClinVar Variation Id:
2803085
ClinVar RCV Id:
RCV003627708
dbSNP Id:
rs568025967
ExAC:
12:5020974 C / T
gnomAD v2:
12-5020974-C-T
gnomAD v3:
12-4911808-C-T
gnomAD v4:
12-4911808-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4911808C>T , CM000674.2:g.4911808C>T | GRCh38 |
| NC_000012.11:g.5020974C>T , CM000674.1:g.5020974C>T | GRCh37 |
| NC_000012.10:g.4891235C>T | NCBI36 |
| NG_011815.1:g.6902C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382545.5:c.430C>T MANE Select | ENSP00000371985.3:p.Leu144= | |
| ENST00000543874.3:n.105+1336C>T | ||
| ENST00000639306.1:c.268C>T | ENSP00000492506.1:p.Leu90= | |
| ENST00000382545.3:c.430C>T | ENSP00000371985.3:p.Leu144= | |
| ENST00000541095.1:n.105+1336C>T | ||
| ENST00000543874.2:n.96+1336C>T | ||
| NM_000217.2:c.430C>T | NP_000208.2:p.Leu144= | |
| NM_000217.3:c.430C>T MANE Select | NP_000208.2:p.Leu144= |