Linked Data
ClinVar Variation Id:
2515117
ClinVar RCV Id:
RCV003270013
dbSNP Id:
rs534164809
ExAC:
17:4836611 G / A
gnomAD v2:
17-4836611-G-A
gnomAD v3:
17-4933316-G-A
gnomAD v4:
17-4933316-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4933316G>A , CM000679.2:g.4933316G>A | GRCh38 |
| NC_000017.10:g.4836611G>A , CM000679.1:g.4836611G>A | GRCh37 |
| NC_000017.9:g.4777391G>A | NCBI36 |
| NG_008767.2:g.6022G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329125.6:c.712G>A (GP1BA) MANE Select | ENSP00000329380.5:p.Asp238Asn | |
| ENST00000649830.1:c.-888+1026C>T (CHRNE) | ENSP00000496907.1:n.-888+1026C>T | |
| ENST00000329125.5:c.712G>A (GP1BA) | ENSP00000329380.5:p.Asp238Asn | |
| ENST00000611961.1:c.712G>A (GP1BA) | ENSP00000484439.1:p.Asp238Asn | |
| NM_000173.6:c.712G>A (GP1BA) | NP_000164.5:p.Asp238Asn | |
| NM_000173.7:c.712G>A (GP1BA) MANE Select | NP_000164.5:p.Asp238Asn |