Linked Data
ClinVar Variation Id:
1337896
ClinVar RCV Id:
RCV001822494
dbSNP Id:
rs1403553441
gnomAD v2:
1-172634804-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.172665664C>T , CM000663.2:g.172665664C>T | GRCh38 |
| NC_000001.10:g.172634804C>T , CM000663.1:g.172634804C>T | GRCh37 |
| NC_000001.9:g.170901427C>T | NCBI36 |
| NG_007269.1:g.11620C>T , LRG_58:g.11620C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367721.3:c.494C>T MANE Select | ENSP00000356694.2:p.Thr165Ile | |
| ENST00000340030.4:c.*64C>T | ENSP00000344739.3:n.*64C>T | |
| ENST00000367721.2:c.494C>T | ENSP00000356694.2:p.Thr165Ile | |
| NM_000639.2:c.494C>T | NP_000630.1:p.Thr165Ile | |
| NM_001302746.1:c.*64C>T | NP_001289675.1:n.*64C>T | |
| NM_000639.3:c.494C>T MANE Select | NP_000630.1:p.Thr165Ile | |
| NM_001302746.2:c.*64C>T | NP_001289675.1:n.*64C>T |