Linked Data
ClinVar Variation Id:
1080197
ClinVar RCV Id:
RCV001395723
dbSNP Id:
rs1309785126
gnomAD v2:
6-162864360-C-T
gnomAD v4:
6-162443328-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.162443328C>T , CM000668.2:g.162443328C>T | GRCh38 |
| NC_000006.11:g.162864360C>T , CM000668.1:g.162864360C>T | GRCh37 |
| NC_000006.10:g.162784350C>T | NCBI36 |
| NG_008289.1:g.289475G>A | |
| NG_008289.2:g.289475G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338468.8:c.153G>A | ENSP00000343589.4:p.Arg51= | |
| ENST00000366894.6:c.153G>A | ENSP00000355860.2:p.Arg51= | |
| ENST00000366898.6:c.153G>A MANE Select | ENSP00000355865.1:p.Arg51= | |
| ENST00000648830.1:n.320G>A | ||
| ENST00000673871.1:c.148G>A | ||
| ENST00000674232.1:n.171G>A | ||
| ENST00000674259.1:n.210G>A | ||
| ENST00000674493.1:n.170G>A | ||
| ENST00000674501.1:n.260G>A | ||
| ENST00000338468.7:c.-299G>A | ENSP00000343589.3:n.-299G>A | |
| ENST00000366892.5:c.153G>A | ENSP00000355858.1:p.Arg51= | |
| ENST00000366894.5:c.-180G>A | ENSP00000355860.1:n.-180G>A | |
| ENST00000366896.5:c.153G>A | ENSP00000355862.1:p.Arg51= | |
| ENST00000366897.5:c.153G>A | ENSP00000355863.1:p.Arg51= | |
| ENST00000366898.5:c.153G>A | ENSP00000355865.1:p.Arg51= | |
| ENST00000479615.5:c.-66-180563G>A | ENSP00000434414.1:n.-66-180563G>A | |
| NM_004562.2:c.153G>A | NP_004553.2:p.Arg51= | |
| NM_013987.2:c.153G>A | NP_054642.2:p.Arg51= | |
| NM_013988.2:c.153G>A | NP_054643.2:p.Arg51= | |
| XM_011535863.1:c.153G>A | XP_011534165.1:p.Arg51= | |
| XM_011535864.1:c.153G>A | XP_011534166.1:p.Arg51= | |
| XM_011535865.1:c.153G>A | XP_011534167.1:p.Arg51= | |
| XM_011535866.1:c.153G>A | XP_011534168.1:p.Arg51= | |
| XM_011535867.1:c.153G>A | XP_011534169.1:p.Arg51= | |
| XM_017010908.1:c.267G>A | XP_016866397.1:p.Arg89= | |
| XM_017010909.2:c.-66-180563G>A | XP_016866398.1:n.-66-180563G>A | |
| XM_024446449.1:c.-66-180563G>A | XP_024302217.1:n.-66-180563G>A | |
| XR_001743443.2:n.259G>A | ||
| NM_004562.3:c.153G>A MANE Select | NP_004553.2:p.Arg51= | |
| NM_013987.3:c.153G>A | NP_054642.2:p.Arg51= | |
| NM_013988.3:c.153G>A | NP_054643.2:p.Arg51= |