Linked Data
ClinVar Variation Id:
906866
dbSNP Id:
rs1410058775
gnomAD v3:
5-148985159-C-A
gnomAD v4:
5-148985159-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.148985159C>A , CM000667.2:g.148985159C>A | GRCh38 |
| NC_000005.9:g.148364722C>A , CM000667.1:g.148364722C>A | GRCh37 |
| NC_000005.8:g.148344915C>A | NCBI36 |
| NG_007947.2:g.83016G>T , LRG_269:g.83016G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000515425.6:c.*19552G>T MANE Select | ENSP00000423660.1:n.*19552G>T | |
| ENST00000504690.5:c.*12+18567G>T | ENSP00000425627.1:n.*12+18567G>T | |
| ENST00000510350.1:n.231+21722G>T | ||
| NM_024577.3:c.*19552G>T , LRG_269t1:c.*19552G>T | NP_078853.2:n.*19552G>T | |
| NM_024577.4:c.*19552G>T MANE Select | NP_078853.2:n.*19552G>T |