Linked Data
ClinVar Variation Id:
1093112
ClinVar RCV Id:
RCV001413189
dbSNP Id:
rs2148184619
MyVariant Identifiers:
chr1:g.21900237G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.21573744G>A , CM000663.2:g.21573744G>A | GRCh38 |
| NC_000001.10:g.21900237G>A , CM000663.1:g.21900237G>A | GRCh37 |
| NC_000001.9:g.21772824G>A | NCBI36 |
| NG_008940.1:g.69380G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374840.8:c.942G>A MANE Select | ENSP00000363973.3:p.Val314= | |
| ENST00000374830.2:c.73-1989G>A | ||
| ENST00000374832.5:c.942G>A | ENSP00000363965.1:p.Val314= | |
| ENST00000374840.7:c.942G>A | ENSP00000363973.3:p.Val314= | |
| ENST00000539907.5:c.711G>A | ENSP00000437674.1:p.Val237= | |
| ENST00000540617.5:c.777G>A | ENSP00000442672.1:p.Val259= | |
| NM_000478.4:c.942G>A | NP_000469.3:p.Val314= | |
| NM_001127501.2:c.777G>A | NP_001120973.2:p.Val259= | |
| NM_001177520.1:c.711G>A | NP_001170991.1:p.Val237= | |
| XM_005245818.1:c.942G>A | XP_005245875.1:p.Val314= | |
| XM_005245820.2:c.942G>A | XP_005245877.1:p.Val314= | |
| XM_006710546.1:c.942G>A | XP_006710609.1:p.Val314= | |
| NM_000478.5:c.942G>A | NP_000469.3:p.Val314= | |
| NM_001127501.3:c.777G>A | NP_001120973.2:p.Val259= | |
| NM_001177520.2:c.711G>A | NP_001170991.1:p.Val237= | |
| XM_006710546.3:c.942G>A | XP_006710609.1:p.Val314= | |
| XM_017000903.1:c.786G>A | XP_016856392.1:p.Val262= | |
| NM_000478.6:c.942G>A MANE Select | NP_000469.3:p.Val314= | |
| NM_001127501.4:c.777G>A | NP_001120973.2:p.Val259= | |
| NM_001177520.3:c.711G>A | NP_001170991.1:p.Val237= | |
| NM_001369803.2:c.942G>A | NP_001356732.1:p.Val314= | |
| NM_001369804.2:c.942G>A | NP_001356733.1:p.Val314= | |
| NM_001369805.2:c.942G>A | NP_001356734.1:p.Val314= |