Linked Data
ClinVar Variation Id:
2959655
ClinVar RCV Id:
RCV003811830
dbSNP Id:
rs1185406817
gnomAD v3:
17-10639789-A-C
gnomAD v4:
17-10639789-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.10639789A>C , CM000679.2:g.10639789A>C | GRCh38 |
| NC_000017.10:g.10543106A>C , CM000679.1:g.10543106A>C | GRCh37 |
| NC_000017.9:g.10483831A>C | NCBI36 |
| NG_011537.1:g.22510T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000583535.6:c.2696T>G MANE Select | ENSP00000464317.1:p.Leu899Trp | |
| ENST00000583535.5:c.2696T>G | ENSP00000464317.1:p.Leu899Trp | |
| NM_002470.3:c.2696T>G | NP_002461.2:p.Leu899Trp | |
| XM_011523870.1:c.2696T>G | XP_011522172.1:p.Leu899Trp | |
| XM_011523871.1:c.2696T>G | XP_011522173.1:p.Leu899Trp | |
| XM_011523872.1:c.2696T>G | XP_011522174.1:p.Leu899Trp | |
| XM_011523870.3:c.2696T>G | XP_011522172.1:p.Leu899Trp | |
| XM_011523871.2:c.2696T>G | XP_011522173.1:p.Leu899Trp | |
| NM_002470.4:c.2696T>G MANE Select | NP_002461.2:p.Leu899Trp |