Linked Data
ClinVar Variation Id:
987776
ClinVar RCV Id:
RCV001269075
dbSNP Id:
rs1876618843
ERepo:
CA16020787/MONDO:0009861/006
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102877460A>C , CM000674.2:g.102877460A>C | GRCh38 |
| NC_000012.11:g.103271238A>C , CM000674.1:g.103271238A>C | GRCh37 |
| NC_000012.10:g.101795368A>C | NCBI36 |
| NG_008690.1:g.45143T>G | |
| NG_008690.2:g.85951T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000553106.6:c.441+2T>G MANE Select | ENSP00000448059.1:n.441+2T>G | |
| ENST00000307000.7:c.426+2T>G | ENSP00000303500.2:n.426+2T>G | |
| ENST00000549111.5:n.537+2T>G | ||
| ENST00000550978.6:c.427T>G | ||
| ENST00000551988.5:n.530+2T>G | ||
| ENST00000553106.5:c.441+2T>G | ENSP00000448059.1:n.441+2T>G | |
| NM_000277.1:c.441+2T>G | NP_000268.1:n.441+2T>G | |
| XM_011538422.1:c.441+2T>G | XP_011536724.1:n.441+2T>G | |
| NM_000277.2:c.441+2T>G | NP_000268.1:n.441+2T>G | |
| NM_001354304.1:c.441+2T>G | NP_001341233.1:n.441+2T>G | |
| XM_017019370.2:c.441+2T>G | XP_016874859.1:n.441+2T>G | |
| NM_000277.3:c.441+2T>G MANE Select | NP_000268.1:n.441+2T>G | |
| NM_001354304.2:c.441+2T>G | NP_001341233.1:n.441+2T>G |