Linked Data
ClinVar Variation Id:
285963
dbSNP Id:
rs774323736
ExAC:
2:220286196 C / T
gnomAD v2:
2-220286196-C-T
gnomAD v3:
2-219421474-C-T
gnomAD v4:
2-219421474-C-T
COSMIC:
COSM6232977
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.219421474C>T , CM000664.2:g.219421474C>T | GRCh38 |
| NC_000002.11:g.220286196C>T , CM000664.1:g.220286196C>T | GRCh37 |
| NC_000002.10:g.219994440C>T | NCBI36 |
| NG_008043.1:g.8098C>T , LRG_380:g.8098C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000477226.6:n.632C>T | ||
| ENST00000683013.1:n.546C>T | ||
| ENST00000373960.4:c.1158C>T MANE Select | ENSP00000363071.3:p.Arg386= | |
| ENST00000373960.3:c.1158C>T | ENSP00000363071.3:p.Arg386= | |
| ENST00000477226.5:n.630C>T | ||
| ENST00000492726.1:n.553C>T | ||
| NM_001927.3:c.1158C>T , LRG_380t1:c.1158C>T | NP_001918.3:p.Arg386= | |
| NM_001927.4:c.1158C>T MANE Select | NP_001918.3:p.Arg386= | |
| NM_001382708.1:c.1155C>T | NP_001369637.1:p.Arg385= | |
| NM_001382709.1:c.736-10C>T | NP_001369638.1:n.736-10C>T | |
| NM_001382710.1:c.1089C>T | NP_001369639.1:p.Arg363= | |
| NM_001382711.1:c.1137C>T | NP_001369640.1:p.Arg379= | |
| NM_001382712.1:c.1158C>T | NP_001369641.1:p.Arg386= | |
| NM_001382713.1:c.888C>T | NP_001369642.1:p.Arg296= |