Linked Data
ClinVar Variation Id:
427103
ClinVar RCV Id:
RCV000489336
dbSNP Id:
rs1005670966
gnomAD v4:
18-12351097-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.12351097G>A , CM000680.2:g.12351097G>A | GRCh38 |
| NC_000018.9:g.12351096G>A , CM000680.1:g.12351096G>A | GRCh37 |
| NC_000018.8:g.12341096G>A | NCBI36 |
| NG_023361.1:g.31180C>T , LRG_666:g.31180C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000687337.1:c.*1136C>T | ENSP00000508998.1:n.*1136C>T | |
| ENST00000688199.1:c.1402C>T | ENSP00000510237.1:p.Pro468Ser | |
| ENST00000691179.1:c.1465C>T | ENSP00000509010.1:p.Pro489Ser | |
| ENST00000691970.1:c.*917C>T | ENSP00000508440.1:n.*917C>T | |
| ENST00000692497.1:c.1540C>T | ENSP00000509870.1:p.Pro514Ser | |
| ENST00000692988.1:n.1358C>T | ||
| ENST00000269143.8:c.1540C>T MANE Select | ENSP00000269143.2:p.Pro514Ser | |
| ENST00000269143.7:c.1540C>T | ENSP00000269143.2:p.Pro514Ser | |
| NM_006796.2:c.1540C>T , LRG_666t1:c.1540C>T | NP_006787.2:p.Pro514Ser | |
| XM_011525601.1:c.1540C>T | XP_011523903.1:p.Pro514Ser | |
| XM_011525601.3:c.1540C>T | XP_011523903.1:p.Pro514Ser | |
| NM_006796.3:c.1540C>T MANE Select | NP_006787.2:p.Pro514Ser |