Linked Data
ClinVar Variation Id:
2814235
ClinVar RCV Id:
RCV003680829
dbSNP Id:
rs1570269636
MyVariant Identifiers:
chr1:g.21887633T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.21561140T>G , CM000663.2:g.21561140T>G | GRCh38 |
| NC_000001.10:g.21887633T>G , CM000663.1:g.21887633T>G | GRCh37 |
| NC_000001.9:g.21760220T>G | NCBI36 |
| NG_008940.1:g.56776T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374840.8:c.225T>G MANE Select | ENSP00000363973.3:p.Gly75= | |
| ENST00000374832.5:c.225T>G | ENSP00000363965.1:p.Gly75= | |
| ENST00000374840.7:c.225T>G | ENSP00000363973.3:p.Gly75= | |
| ENST00000468526.1:n.285T>G | ||
| ENST00000539907.5:c.66+395T>G | ENSP00000437674.1:n.66+395T>G | |
| ENST00000540617.5:c.60T>G | ENSP00000442672.1:p.Gly20= | |
| NM_000478.4:c.225T>G | NP_000469.3:p.Gly75= | |
| NM_001127501.2:c.60T>G | NP_001120973.2:p.Gly20= | |
| NM_001177520.1:c.66+395T>G | NP_001170991.1:n.66+395T>G | |
| XM_005245818.1:c.225T>G | XP_005245875.1:p.Gly75= | |
| XM_005245820.2:c.225T>G | XP_005245877.1:p.Gly75= | |
| XM_006710546.1:c.225T>G | XP_006710609.1:p.Gly75= | |
| NM_000478.5:c.225T>G | NP_000469.3:p.Gly75= | |
| NM_001127501.3:c.60T>G | NP_001120973.2:p.Gly20= | |
| NM_001177520.2:c.66+395T>G | NP_001170991.1:n.66+395T>G | |
| XM_006710546.3:c.225T>G | XP_006710609.1:p.Gly75= | |
| XM_017000903.1:c.69T>G | XP_016856392.1:p.Gly23= | |
| NM_000478.6:c.225T>G MANE Select | NP_000469.3:p.Gly75= | |
| NM_001127501.4:c.60T>G | NP_001120973.2:p.Gly20= | |
| NM_001177520.3:c.66+395T>G | NP_001170991.1:n.66+395T>G | |
| NM_001369803.2:c.225T>G | NP_001356732.1:p.Gly75= | |
| NM_001369804.2:c.225T>G | NP_001356733.1:p.Gly75= | |
| NM_001369805.2:c.225T>G | NP_001356734.1:p.Gly75= |