Linked Data
ClinVar Variation Id:
2936158
ClinVar RCV Id:
RCV003796444
dbSNP Id:
rs1244196303
gnomAD v2:
15-48766588-G-T
gnomAD v4:
15-48474391-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48474391G>T , CM000677.2:g.48474391G>T | GRCh38 |
| NC_000015.9:g.48766588G>T , CM000677.1:g.48766588G>T | GRCh37 |
| NC_000015.8:g.46553880G>T | NCBI36 |
| NG_008805.2:g.176398C>A , LRG_778:g.176398C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.4088-14C>A | ENSP00000453958.2:n.4088-14C>A | |
| ENST00000674301.2:c.4088-14C>A | ENSP00000501333.2:n.4088-14C>A | |
| ENST00000684448.1:n.2762-14C>A | ||
| ENST00000316623.10:c.4088-14C>A MANE Select | ENSP00000325527.5:n.4088-14C>A | |
| ENST00000316623.9:c.4088-14C>A | ENSP00000325527.5:n.4088-14C>A | |
| ENST00000537463.6:c.760-14C>A | ENSP00000440294.2:n.760-14C>A | |
| NM_000138.4:c.4088-14C>A , LRG_778t1:c.4088-14C>A | NP_000129.3:n.4088-14C>A | |
| NM_000138.5:c.4088-14C>A MANE Select | NP_000129.3:n.4088-14C>A |