Linked Data
ClinVar Variation Id:
2647278
ClinVar RCV Id:
RCV003419585
dbSNP Id:
rs779062552
ExAC:
17:4836470 G / A
gnomAD v2:
17-4836470-G-A
gnomAD v4:
17-4933175-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4933175G>A , CM000679.2:g.4933175G>A | GRCh38 |
| NC_000017.10:g.4836470G>A , CM000679.1:g.4836470G>A | GRCh37 |
| NC_000017.9:g.4777250G>A | NCBI36 |
| NG_008767.2:g.5881G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329125.6:c.571G>A (GP1BA) MANE Select | ENSP00000329380.5:p.Asp191Asn | |
| ENST00000649830.1:c.-888+1167C>T (CHRNE) | ENSP00000496907.1:n.-888+1167C>T | |
| ENST00000329125.5:c.571G>A (GP1BA) | ENSP00000329380.5:p.Asp191Asn | |
| ENST00000611961.1:c.571G>A (GP1BA) | ENSP00000484439.1:p.Asp191Asn | |
| NM_000173.6:c.571G>A (GP1BA) | NP_000164.5:p.Asp191Asn | |
| NM_000173.7:c.571G>A (GP1BA) MANE Select | NP_000164.5:p.Asp191Asn |