Linked Data
ClinVar Variation Id:
1327497
ClinVar RCV Id:
RCV001789725
dbSNP Id:
rs2124790604
MutSpliceDB:
CA339268869
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.26731605G>C , CM000663.2:g.26731605G>C | GRCh38 |
| NC_000001.10:g.27058096G>C , CM000663.1:g.27058096G>C | GRCh37 |
| NC_000001.9:g.26930683G>C | NCBI36 |
| NG_029965.1:g.40575G>C , LRG_875:g.40575G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000324856.13:c.1803+1G>C MANE Select | ENSP00000320485.7:n.1803+1G>C | |
| ENST00000374152.7:c.654+1G>C | ENSP00000363267.2:n.654+1G>C | |
| ENST00000430799.7:c.654+1G>C | ENSP00000390317.3:n.654+1G>C | |
| ENST00000636219.1:c.660+1G>C | ENSP00000489842.1:n.660+1G>C | |
| ENST00000324856.11:c.1803+1G>C | ENSP00000320485.7:n.1803+1G>C | |
| ENST00000374152.6:c.654+1G>C | ENSP00000363267.2:n.654+1G>C | |
| ENST00000457599.6:c.1803+1G>C | ENSP00000387636.2:n.1803+1G>C | |
| ENST00000615191.4:c.654+1G>C | ENSP00000478955.1:n.654+1G>C | |
| NM_006015.4:c.1803+1G>C , LRG_875t1:c.1803+1G>C | NP_006006.3:n.1803+1G>C | |
| NM_139135.2:c.1803+1G>C | NP_624361.1:n.1803+1G>C | |
| NM_006015.5:c.1803+1G>C | NP_006006.3:n.1803+1G>C | |
| NM_139135.3:c.1803+1G>C | NP_624361.1:n.1803+1G>C | |
| NM_006015.6:c.1803+1G>C MANE Select | NP_006006.3:n.1803+1G>C | |
| NM_139135.4:c.1803+1G>C | NP_624361.1:n.1803+1G>C |