Linked Data
ClinVar Variation Id:
36745
ClinVar RCV Id:
RCV000036768
RCV000252666
RCV000272540
RCV001093868
RCV000769786
RCV001530065
RCV001841543
RCV003996141
dbSNP Id:
rs193922628
ExAC:
1:237778014 C / T
gnomAD v2:
1-237778014-C-T
gnomAD v3:
1-237614714-C-T
gnomAD v4:
1-237614714-C-T
PubMed:
PMID:24503780
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.237614714C>T , CM000663.2:g.237614714C>T | GRCh38 |
| NC_000001.10:g.237778014C>T , CM000663.1:g.237778014C>T | GRCh37 |
| NC_000001.9:g.235844637C>T | NCBI36 |
| NG_008799.2:g.577313C>T | |
| NG_008799.3:g.577531C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000609119.2:c.5586C>T | ENSP00000499659.2:p.Asp1862= | |
| ENST00000659194.3:c.5586C>T | ENSP00000499653.3:p.Asp1862= | |
| ENST00000660292.2:c.5586C>T | ENSP00000499787.2:p.Asp1862= | |
| ENST00000366574.7:c.5586C>T MANE Select | ENSP00000355533.2:p.Asp1862= | |
| ENST00000360064.7:c.5538C>T | ENSP00000353174.7:p.Asp1846= | |
| ENST00000366574.6:c.5586C>T | ENSP00000355533.2:p.Asp1862= | |
| NM_001035.2:c.5586C>T | NP_001026.2:p.Asp1862= | |
| XM_006711802.2:c.5616C>T | XP_006711865.1:p.Asp1872= | |
| XM_006711803.2:c.5613C>T | XP_006711866.1:p.Asp1871= | |
| XM_006711804.2:c.5616C>T | XP_006711867.1:p.Asp1872= | |
| XM_006711805.2:c.5586C>T | XP_006711868.1:p.Asp1862= | |
| XM_006711806.2:c.5616C>T | XP_006711869.1:p.Asp1872= | |
| XM_006711807.2:c.5616C>T | XP_006711870.1:p.Asp1872= | |
| XM_006711808.2:c.5616C>T | XP_006711871.1:p.Asp1872= | |
| XM_006711809.2:c.5616C>T | XP_006711872.1:p.Asp1872= | |
| XM_006711810.2:c.5583C>T | XP_006711873.1:p.Asp1861= | |
| XR_949152.1:n.5897C>T | ||
| XM_006711802.3:c.5616C>T | XP_006711865.1:p.Asp1872= | |
| XM_006711803.3:c.5613C>T | XP_006711866.1:p.Asp1871= | |
| XM_006711804.3:c.5616C>T | XP_006711867.1:p.Asp1872= | |
| XM_006711805.3:c.5586C>T | XP_006711868.1:p.Asp1862= | |
| XM_006711806.3:c.5616C>T | XP_006711869.1:p.Asp1872= | |
| XM_006711807.3:c.5616C>T | XP_006711870.1:p.Asp1872= | |
| XM_006711808.3:c.5616C>T | XP_006711871.1:p.Asp1872= | |
| XM_006711810.3:c.5583C>T | XP_006711873.1:p.Asp1861= | |
| XM_017002028.1:c.5595C>T | XP_016857517.1:p.Asp1865= | |
| XR_002957299.1:n.5930C>T | ||
| XR_949152.2:n.5930C>T | ||
| NM_001035.3:c.5586C>T MANE Select | NP_001026.2:p.Asp1862= |