Linked Data
ClinVar Variation Id:
979114
dbSNP Id:
rs745990205
ExAC:
11:2869084 G / A
gnomAD v2:
11-2869084-G-A
gnomAD v3:
11-2847854-G-A
gnomAD v4:
11-2847854-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2847854G>A , CM000673.2:g.2847854G>A | GRCh38 |
| NC_000011.9:g.2869084G>A , CM000673.1:g.2869084G>A | GRCh37 |
| NC_000011.8:g.2825660G>A | NCBI36 |
| NG_008935.1:g.407864G>A , LRG_287:g.407864G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496887.7:c.1525G>A (KCNQ1) | ENSP00000434560.2:p.Gly509Ser | |
| ENST00000155840.12:c.1882G>A (KCNQ1) MANE Select | ENSP00000155840.2:p.Gly628Ser | |
| ENST00000335475.6:c.1501G>A (KCNQ1) | ENSP00000334497.5:p.Gly501Ser | |
| ENST00000526095.2:c.286G>A (KCNQ1) | ENSP00000494939.1:p.Gly96Ser | |
| ENST00000155840.9:c.1882G>A (KCNQ1) | ENSP00000155840.2:p.Gly628Ser | |
| ENST00000335475.5:c.1501G>A (KCNQ1) | ENSP00000334497.5:p.Gly501Ser | |
| ENST00000526095.1:n.389G>A (KCNQ1) | ||
| NM_000218.2:c.1882G>A , LRG_287t1:c.1882G>A (KCNQ1) | NP_000209.2:p.Gly628Ser | |
| NM_181798.1:c.1501G>A , LRG_287t2:c.1501G>A (KCNQ1) | NP_861463.1:p.Gly501Ser | |
| NR_130721.1:n.778-7412C>T (KCNQ1-AS1) | ||
| NM_000218.3:c.1882G>A (KCNQ1) MANE Select | NP_000209.2:p.Gly628Ser |