Linked Data
ClinVar Variation Id:
246037
dbSNP Id:
rs766484755
ExAC:
16:81388292 G / T
gnomAD v2:
16-81388292-G-T
gnomAD v4:
16-81354687-G-T
COSMIC:
COSM6079874
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.81354687G>T , CM000678.2:g.81354687G>T | GRCh38 |
| NC_000016.9:g.81388292G>T , CM000678.1:g.81388292G>T | GRCh37 |
| NC_000016.8:g.79945793G>T | NCBI36 |
| NG_009007.1:g.44722G>T , LRG_242:g.44722G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648349.2:c.*273G>T | ENSP00000498114.1:n.*273G>T | |
| ENST00000648994.2:c.565G>T MANE Select | ENSP00000497351.1:p.Val189Phe | |
| ENST00000650388.1:c.168-2098G>T | ENSP00000498081.1:n.168-2098G>T | |
| ENST00000674788.1:n.690G>T | ||
| ENST00000568107.2:c.565G>T | ENSP00000476795.1:p.Val189Phe | |
| NM_022041.3:c.565G>T , LRG_242t1:c.565G>T | NP_071324.1:p.Val189Phe | |
| XM_017023734.1:c.-75G>T | XP_016879223.1:n.-75G>T | |
| NM_001377486.1:c.-75G>T | NP_001364415.1:n.-75G>T | |
| NM_022041.4:c.565G>T MANE Select | NP_071324.1:p.Val189Phe |