Linked Data
ClinVar Variation Id:
1292423
ClinVar RCV Id:
RCV001714442
dbSNP Id:
rs1678607
gnomAD v2:
3-10188428-T-G
gnomAD v3:
3-10146744-T-G
gnomAD v4:
3-10146744-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10146744T>G , CM000665.2:g.10146744T>G | GRCh38 |
| NC_000003.11:g.10188428T>G , CM000665.1:g.10188428T>G | GRCh37 |
| NC_000003.10:g.10163428T>G | NCBI36 |
| NG_008212.3:g.10110T>G , LRG_322:g.10110T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696142.1:c.*140+108T>G | ENSP00000512434.1:n.*140+108T>G | |
| ENST00000696143.1:c.600-3043T>G | ENSP00000512435.1:n.600-3043T>G | |
| ENST00000696153.1:c.463+108T>G | ENSP00000512444.1:n.463+108T>G | |
| ENST00000256474.3:c.463+108T>G MANE Select | ENSP00000256474.3:n.463+108T>G | |
| ENST00000256474.2:c.463+108T>G | ENSP00000256474.2:n.463+108T>G | |
| ENST00000345392.2:c.341-3043T>G | ENSP00000344757.2:n.341-3043T>G | |
| ENST00000477538.1:n.599+108T>G | ||
| NM_000551.3:c.463+108T>G , LRG_322t1:c.463+108T>G | NP_000542.1:n.463+108T>G | |
| NM_198156.2:c.341-3043T>G | NP_937799.1:n.341-3043T>G | |
| NM_001354723.1:c.*18-3043T>G | NP_001341652.1:n.*18-3043T>G | |
| NM_000551.4:c.463+108T>G MANE Select | NP_000542.1:n.463+108T>G | |
| NM_001354723.2:c.*18-3043T>G | NP_001341652.1:n.*18-3043T>G | |
| NM_198156.3:c.341-3043T>G | NP_937799.1:n.341-3043T>G |