Linked Data
ClinVar Variation Id:
418427
dbSNP Id:
rs185112635
ExAC:
19:40903367 G / A
gnomAD v2:
19-40903367-G-A
gnomAD v3:
19-40397460-G-A
gnomAD v4:
19-40397460-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.40397460G>A , CM000681.2:g.40397460G>A | GRCh38 |
| NC_000019.9:g.40903367G>A , CM000681.1:g.40903367G>A | GRCh37 |
| NC_000019.8:g.45595207G>A | NCBI36 |
| NG_007979.1:g.20905C>T , LRG_265:g.20905C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000324001.8:c.892C>T MANE Select | ENSP00000326018.6:p.Pro298Ser | |
| ENST00000673881.1:c.475C>T | ENSP00000501070.1:p.Pro159Ser | |
| ENST00000674005.2:c.1177C>T | ENSP00000501261.1:p.Pro393Ser | |
| ENST00000674773.1:c.475C>T | ENSP00000502579.1:p.Pro159Ser | |
| ENST00000675517.1:c.767C>T | ||
| ENST00000676076.1:c.753C>T | ||
| ENST00000676260.1:c.854C>T | ||
| ENST00000676316.1:c.779C>T | ||
| ENST00000291825.11:c.*1097C>T | ENSP00000291825.6:n.*1097C>T | |
| ENST00000324001.7:c.892C>T | ENSP00000326018.6:p.Pro298Ser | |
| NM_020956.2:c.*1097C>T , LRG_265t1:c.*1097C>T | NP_066007.1:n.*1097C>T | |
| NM_181882.2:c.892C>T , LRG_265t2:c.892C>T | NP_870998.2:p.Pro298Ser | |
| XM_011527171.1:c.892C>T | XP_011525473.1:p.Pro298Ser | |
| XM_011527171.2:c.892C>T | XP_011525473.1:p.Pro298Ser | |
| XM_017027046.1:c.790C>T | XP_016882535.1:p.Pro264Ser | |
| XM_017027047.1:c.790C>T | XP_016882536.1:p.Pro264Ser | |
| NM_181882.3:c.892C>T MANE Select | NP_870998.2:p.Pro298Ser |