Linked Data
ClinVar Variation Id:
2143893
ClinVar RCV Id:
RCV003062827
dbSNP Id:
rs757315161
gnomAD v3:
15-89328758-C-T
gnomAD v4:
15-89328758-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89328758C>T , CM000677.2:g.89328758C>T | GRCh38 |
| NC_000015.9:g.89871989C>T , CM000677.1:g.89871989C>T | GRCh37 |
| NC_000015.8:g.87672993C>T | NCBI36 |
| NG_008218.1:g.11038G>A | |
| NG_008218.2:g.11038G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000636937.2:c.1097G>A | ENSP00000516154.1:p.Gly366Glu | |
| ENST00000268124.11:c.1097G>A MANE Select | ENSP00000268124.5:p.Gly366Glu | |
| ENST00000530292.3:c.698G>A | ENSP00000432885.2:p.Gly233Glu | |
| ENST00000635986.2:c.1097G>A | ENSP00000490653.2:p.Gly366Glu | |
| ENST00000636774.1:c.1097G>A | ENSP00000489799.1:p.Gly366Glu | |
| ENST00000637264.1:c.169G>A | ||
| ENST00000666746.1:c.754G>A | ||
| ENST00000672071.1:n.1295G>A | ||
| ENST00000672923.2:n.94G>A | ||
| ENST00000268124.9:c.1097G>A | ENSP00000268124.5:p.Gly366Glu | |
| ENST00000442287.6:c.1097G>A | ENSP00000399851.2:p.Gly366Glu | |
| ENST00000631044.2:c.*480G>A | ENSP00000486730.1:n.*480G>A | |
| NM_001126131.1:c.1097G>A | NP_001119603.1:p.Gly366Glu | |
| NM_002693.2:c.1097G>A | NP_002684.1:p.Gly366Glu | |
| NM_001126131.2:c.1097G>A | NP_001119603.1:p.Gly366Glu | |
| NM_002693.3:c.1097G>A MANE Select | NP_002684.1:p.Gly366Glu |