Linked Data
dbSNP Id:
rs540032372
ExAC:
15:48703139 C / T
gnomAD v2:
15-48703139-C-T
gnomAD v3:
15-48410942-C-T
gnomAD v4:
15-48410942-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48410942C>T , CM000677.2:g.48410942C>T | GRCh38 |
| NC_000015.9:g.48703139C>T , CM000677.1:g.48703139C>T | GRCh37 |
| NC_000015.8:g.46490431C>T | NCBI36 |
| NG_008805.2:g.239847G>A , LRG_778:g.239847G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.*1472G>A | ENSP00000453958.2:n.*1472G>A | |
| ENST00000682158.1:n.2045G>A | ||
| ENST00000682170.1:n.2845G>A | ||
| ENST00000682767.1:n.1961G>A | ||
| ENST00000316623.10:c.*48G>A MANE Select | ENSP00000325527.5:n.*48G>A | |
| ENST00000316623.9:c.*48G>A | ENSP00000325527.5:n.*48G>A | |
| ENST00000559133.5:c.4033G>A | ||
| NM_000138.4:c.*48G>A , LRG_778t1:c.*48G>A | NP_000129.3:n.*48G>A | |
| NM_000138.5:c.*48G>A MANE Select | NP_000129.3:n.*48G>A |