Linked Data
ClinVar Variation Id:
1604592
ClinVar RCV Id:
RCV002134709
dbSNP Id:
rs1276497226
gnomAD v3:
17-42536326-C-G
gnomAD v4:
17-42536326-C-G
MyVariant Identifiers:
chr17:g.40688344C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42536326C>G , CM000679.2:g.42536326C>G | GRCh38 |
| NC_000017.10:g.40688344C>G , CM000679.1:g.40688344C>G | GRCh37 |
| NC_000017.9:g.37941870C>G | NCBI36 |
| NG_011552.1:g.5394C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.54C>G MANE Select | ENSP00000225927.1:p.Ala18= | |
| ENST00000225927.6:c.54C>G | ENSP00000225927.1:p.Ala18= | |
| NM_000263.3:c.54C>G | NP_000254.2:p.Ala18= | |
| XM_024450771.1:c.54C>G | XP_024306539.1:p.Ala18= | |
| NM_000263.4:c.54C>G MANE Select | NP_000254.2:p.Ala18= |