Linked Data
ClinVar Variation Id:
462106
ClinVar RCV Id:
RCV000526461
dbSNP Id:
rs143485066
ExAC:
17:80037464 C / T
gnomAD v2:
17-80037464-C-T
gnomAD v3:
17-82079588-C-T
gnomAD v4:
17-82079588-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.82079588C>T , CM000679.2:g.82079588C>T | GRCh38 |
| NC_000017.10:g.80037464C>T , CM000679.1:g.80037464C>T | GRCh37 |
| NC_000017.9:g.77630753C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306749.4:c.7167G>A MANE Select | ENSP00000304592.2:p.Pro2389= | |
| ENST00000306749.3:c.7167G>A | ENSP00000304592.2:p.Pro2389= | |
| ENST00000578424.2:n.446G>A | ||
| ENST00000580382.1:c.337G>A | ||
| ENST00000584610.2:n.342G>A | ||
| ENST00000634990.1:c.7161G>A | ENSP00000488964.1:p.Pro2387= | |
| NM_004104.4:c.7167G>A | NP_004095.4:p.Pro2389= | |
| XM_011523538.1:c.7167G>A | XP_011521840.1:p.Pro2389= | |
| XM_011523538.2:c.7167G>A | XP_011521840.1:p.Pro2389= | |
| NM_004104.5:c.7167G>A MANE Select | NP_004095.4:p.Pro2389= |