Linked Data
ClinVar Variation Id:
444468
dbSNP Id:
rs150244426
ExAC:
19:40903037 G / A
gnomAD v2:
19-40903037-G-A
gnomAD v3:
19-40397130-G-A
gnomAD v4:
19-40397130-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.40397130G>A , CM000681.2:g.40397130G>A | GRCh38 |
| NC_000019.9:g.40903037G>A , CM000681.1:g.40903037G>A | GRCh37 |
| NC_000019.8:g.45594877G>A | NCBI36 |
| NG_007979.1:g.21235C>T , LRG_265:g.21235C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000324001.8:c.1222C>T MANE Select | ENSP00000326018.6:p.Pro408Ser | |
| ENST00000673881.1:c.805C>T | ENSP00000501070.1:p.Pro269Ser | |
| ENST00000674005.2:c.1507C>T | ENSP00000501261.1:p.Pro503Ser | |
| ENST00000674773.1:c.805C>T | ENSP00000502579.1:p.Pro269Ser | |
| ENST00000675517.1:c.1097C>T | ||
| ENST00000676076.1:c.1083C>T | ||
| ENST00000676260.1:c.1184C>T | ||
| ENST00000676316.1:c.1109C>T | ||
| ENST00000291825.11:c.*1427C>T | ENSP00000291825.6:n.*1427C>T | |
| ENST00000324001.7:c.1222C>T | ENSP00000326018.6:p.Pro408Ser | |
| NM_020956.2:c.*1427C>T , LRG_265t1:c.*1427C>T | NP_066007.1:n.*1427C>T | |
| NM_181882.2:c.1222C>T , LRG_265t2:c.1222C>T | NP_870998.2:p.Pro408Ser | |
| XM_011527171.1:c.1222C>T | XP_011525473.1:p.Pro408Ser | |
| XM_011527171.2:c.1222C>T | XP_011525473.1:p.Pro408Ser | |
| XM_017027046.1:c.1120C>T | XP_016882535.1:p.Pro374Ser | |
| XM_017027047.1:c.1120C>T | XP_016882536.1:p.Pro374Ser | |
| NM_181882.3:c.1222C>T MANE Select | NP_870998.2:p.Pro408Ser |