Linked Data
ClinVar Variation Id:
380618
dbSNP Id:
rs747274959
ExAC:
15:48786454 G / A
gnomAD v2:
15-48786454-G-A
gnomAD v4:
15-48494257-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48494257G>A , CM000677.2:g.48494257G>A | GRCh38 |
| NC_000015.9:g.48786454G>A , CM000677.1:g.48786454G>A | GRCh37 |
| NC_000015.8:g.46573746G>A | NCBI36 |
| NG_008805.2:g.156532C>T , LRG_778:g.156532C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.2678-3C>T | ENSP00000453958.2:n.2678-3C>T | |
| ENST00000674301.2:c.2678-3C>T | ENSP00000501333.2:n.2678-3C>T | |
| ENST00000684448.1:n.1352-3C>T | ||
| ENST00000316623.10:c.2678-3C>T MANE Select | ENSP00000325527.5:n.2678-3C>T | |
| ENST00000316623.9:c.2678-3C>T | ENSP00000325527.5:n.2678-3C>T | |
| ENST00000537463.6:c.637-19607C>T | ENSP00000440294.2:n.637-19607C>T | |
| NM_000138.4:c.2678-3C>T , LRG_778t1:c.2678-3C>T | NP_000129.3:n.2678-3C>T | |
| NM_000138.5:c.2678-3C>T MANE Select | NP_000129.3:n.2678-3C>T |