Linked Data
ClinVar Variation Id:
845113
ClinVar RCV Id:
RCV001048115
dbSNP Id:
rs1697260624
gnomAD v4:
3-42685782-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.42685782G>A , CM000665.2:g.42685782G>A | GRCh38 |
| NC_000003.11:g.42727274G>A , CM000665.1:g.42727274G>A | GRCh37 |
| NC_000003.10:g.42702278G>A | NCBI36 |
| NG_033035.1:g.5264G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000287777.5:c.164G>A MANE Select | ENSP00000287777.4:p.Ser55Asn | |
| ENST00000287777.4:c.164G>A | ENSP00000287777.4:p.Ser55Asn | |
| NM_152393.3:c.164G>A | NP_689606.2:p.Ser55Asn | |
| XM_005264866.2:c.164G>A | XP_005264923.1:p.Ser55Asn | |
| NM_152393.4:c.164G>A MANE Select | NP_689606.2:p.Ser55Asn |