Linked Data
ClinVar Variation Id:
1116675
ClinVar RCV Id:
RCV001445131
dbSNP Id:
rs750577663
MyVariant Identifiers:
chr19:g.10904477G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10793801G>T , CM000681.2:g.10793801G>T | GRCh38 |
| NC_000019.9:g.10904477G>T , CM000681.1:g.10904477G>T | GRCh37 |
| NC_000019.8:g.10765477G>T | NCBI36 |
| NG_008792.1:g.80723G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682285.1:n.1262G>T | ||
| ENST00000682524.1:n.1262G>T | ||
| ENST00000683738.1:n.1262G>T | ||
| ENST00000355667.11:c.1074G>T | ENSP00000347890.6:p.Gly358= | |
| ENST00000389253.9:c.1074G>T MANE Select | ENSP00000373905.4:p.Gly358= | |
| ENST00000355667.10:c.1074G>T | ENSP00000347890.6:p.Gly358= | |
| ENST00000359692.10:c.1074G>T | ENSP00000352721.6:p.Gly358= | |
| ENST00000389253.8:c.1074G>T | ENSP00000373905.3:p.Gly358= | |
| ENST00000408974.8:c.1074G>T | ENSP00000386192.3:p.Gly358= | |
| ENST00000585892.5:c.1074G>T | ENSP00000468734.1:p.Gly358= | |
| ENST00000587830.2:c.330G>T | ENSP00000466603.2:p.Gly110= | |
| ENST00000591701.5:n.434G>T | ||
| NM_001005360.2:c.1074G>T | NP_001005360.1:p.Gly358= | |
| NM_001005361.2:c.1074G>T | NP_001005361.1:p.Gly358= | |
| NM_001005362.2:c.1074G>T | NP_001005362.1:p.Gly358= | |
| NM_001190716.1:c.1074G>T | NP_001177645.1:p.Gly358= | |
| NM_004945.3:c.1074G>T | NP_004936.2:p.Gly358= | |
| NM_001005361.3:c.1074G>T MANE Select | NP_001005361.1:p.Gly358= | |
| NM_001190716.2:c.1074G>T | NP_001177645.1:p.Gly358= | |
| NM_001005360.3:c.1074G>T | NP_001005360.1:p.Gly358= | |
| NM_001005362.3:c.1074G>T | NP_001005362.1:p.Gly358= | |
| NM_004945.4:c.1074G>T | NP_004936.2:p.Gly358= |