Linked Data
ClinVar Variation Id:
102521
dbSNP Id:
rs62516098
gnomAD v4:
12-102843748-G-T
ERepo:
CA229341/MONDO:0009861/006
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102843748G>T , CM000674.2:g.102843748G>T | GRCh38 |
| NC_000012.11:g.103237526G>T , CM000674.1:g.103237526G>T | GRCh37 |
| NC_000012.10:g.101761656G>T | NCBI36 |
| NG_008690.1:g.78855C>A | |
| NG_008690.2:g.119663C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.1097C>A MANE Select | ENSP00000448059.1:p.Pro366His | |
| ENST00000307000.7:c.1082C>A | ENSP00000303500.2:p.Pro361His | |
| ENST00000549247.6:n.856C>A | ||
| ENST00000551114.2:n.759C>A | ||
| ENST00000553106.5:c.1097C>A | ENSP00000448059.1:p.Pro366His | |
| ENST00000635477.1:c.201C>A | ||
| ENST00000635528.1:n.612C>A | ||
| NM_000277.1:c.1097C>A | NP_000268.1:p.Pro366His | |
| XM_011538422.1:c.1040C>A | XP_011536724.1:p.Pro347His | |
| NM_000277.2:c.1097C>A | NP_000268.1:p.Pro366His | |
| NM_001354304.1:c.1097C>A | NP_001341233.1:p.Pro366His | |
| NM_000277.3:c.1097C>A MANE Select | NP_000268.1:p.Pro366His | |
| NM_001354304.2:c.1097C>A | NP_001341233.1:p.Pro366His |