Linked Data
ClinVar Variation Id:
635232
ClinVar RCV Id:
RCV000786215
dbSNP Id:
rs1558232391
MyVariant Identifiers:
chr1:g.236882202C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.236718902C>T , CM000663.2:g.236718902C>T | GRCh38 |
| NC_000001.10:g.236882202C>T , CM000663.1:g.236882202C>T | GRCh37 |
| NC_000001.9:g.234948825C>T | NCBI36 |
| NG_009081.1:g.37433C>T | |
| NG_009081.2:g.59762C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000542672.7:c.250C>T | ENSP00000443495.1:p.Leu84= | |
| ENST00000492634.7:n.345C>T | ||
| ENST00000682015.1:c.250C>T | ENSP00000506961.1:p.Leu84= | |
| ENST00000682692.1:n.250C>T | ||
| ENST00000682966.1:n.249C>T | ||
| ENST00000683075.1:n.189C>T | ||
| ENST00000683111.1:c.193C>T | ENSP00000507913.1:p.Leu65= | |
| ENST00000684050.1:n.285C>T | ||
| ENST00000684286.1:n.318C>T | ||
| ENST00000684502.1:n.285C>T | ||
| ENST00000366578.6:c.250C>T MANE Select | ENSP00000355537.4:p.Leu84= | |
| ENST00000492634.6:n.345C>T | ||
| ENST00000542672.6:c.250C>T | ENSP00000443495.1:p.Leu84= | |
| ENST00000651091.1:c.193C>T | ENSP00000498677.1:p.Leu65= | |
| ENST00000651187.1:c.34C>T | ENSP00000498348.1:p.Leu12= | |
| ENST00000651275.1:c.235C>T | ENSP00000498926.1:p.Leu79= | |
| ENST00000651786.1:c.250C>T | ENSP00000498364.1:p.Leu84= | |
| ENST00000652096.1:c.250C>T | ENSP00000498896.1:p.Leu84= | |
| ENST00000366578.5:c.250C>T | ENSP00000355537.4:p.Leu84= | |
| ENST00000492634.5:n.397C>T | ||
| ENST00000542672.5:c.250C>T | ENSP00000443495.1:p.Leu84= | |
| ENST00000546208.5:c.-572C>T | ENSP00000438384.2:n.-572C>T | |
| NM_001103.3:c.250C>T | NP_001094.1:p.Leu84= | |
| NM_001278343.1:c.250C>T | NP_001265272.1:p.Leu84= | |
| NM_001278344.1:c.-572C>T | NP_001265273.1:n.-572C>T | |
| NM_001278343.2:c.250C>T | NP_001265272.1:p.Leu84= | |
| NM_001103.4:c.250C>T MANE Select | NP_001094.1:p.Leu84= | |
| NM_001278344.2:c.-572C>T | NP_001265273.1:n.-572C>T |