Linked Data
ClinVar Variation Id:
2165979
dbSNP Id:
rs1475769784
gnomAD v3:
10-87743463-G-A
gnomAD v4:
10-87743463-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87743463G>A , CM000672.2:g.87743463G>A | GRCh38 |
| NC_000010.10:g.89503220G>A , CM000672.1:g.89503220G>A | GRCh37 |
| NC_000010.9:g.89493200G>A | NCBI36 |
| NG_012150.1:g.88745G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000456849.2:c.1313G>A MANE Select | ENSP00000406157.1:p.Gly438Asp | |
| ENST00000361175.8:c.1298G>A | ENSP00000354436.4:p.Gly433Asp | |
| ENST00000456849.1:c.1313G>A | ENSP00000406157.1:p.Gly438Asp | |
| NM_001015880.1:c.1313G>A | NP_001015880.1:p.Gly438Asp | |
| NM_004670.3:c.1298G>A | NP_004661.2:p.Gly433Asp | |
| NM_001015880.2:c.1313G>A MANE Select | NP_001015880.1:p.Gly438Asp | |
| NM_004670.4:c.1298G>A | NP_004661.2:p.Gly433Asp |