Linked Data
dbSNP Id:
rs782262681
ExAC:
22:19164039 C / A
gnomAD v2:
22-19164039-C-A
gnomAD v4:
22-19176526-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.19176526C>A , CM000684.2:g.19176526C>A | GRCh38 |
| NC_000022.10:g.19164039C>A , CM000684.1:g.19164039C>A | GRCh37 |
| NC_000022.9:g.17544039C>A | NCBI36 |
| NG_033863.1:g.7338G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000215882.10:c.748-32G>T MANE Select | ENSP00000215882.5:n.748-32G>T | |
| ENST00000215882.9:c.748-32G>T | ENSP00000215882.5:n.748-32G>T | |
| ENST00000451283.5:c.439-32G>T | ENSP00000401480.1:n.439-32G>T | |
| ENST00000470922.5:n.890-32G>T | ||
| NM_001256534.1:c.769-32G>T | NP_001243463.1:n.769-32G>T | |
| NM_001287387.1:c.439-32G>T | NP_001274316.1:n.439-32G>T | |
| NM_005984.4:c.748-32G>T | NP_005975.1:n.748-32G>T | |
| NR_046298.2:n.799-32G>T | ||
| NM_005984.5:c.748-32G>T MANE Select | NP_005975.1:n.748-32G>T | |
| NM_001256534.2:c.769-32G>T | NP_001243463.1:n.769-32G>T | |
| NM_001287387.2:c.439-32G>T | NP_001274316.1:n.439-32G>T | |
| NR_046298.3:n.672-32G>T |