Linked Data
ClinVar Variation Id:
326188
ClinVar RCV Id:
RCV000349121
dbSNP Id:
rs4797824
gnomAD v2:
18-13884513-C-T
gnomAD v3:
18-13884514-C-T
gnomAD v4:
18-13884514-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.13884514C>T , CM000680.2:g.13884514C>T | GRCh38 |
| NC_000018.9:g.13884513C>T , CM000680.1:g.13884513C>T | GRCh37 |
| NC_000018.8:g.13874513C>T | NCBI36 |
| NG_011819.1:g.36023G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327606.4:c.*111G>A MANE Select | ENSP00000333821.2:n.*111G>A | |
| ENST00000327606.3:c.*111G>A | ENSP00000333821.2:n.*111G>A | |
| NM_000529.2:c.*111G>A MANE Select | NP_000520.1:n.*111G>A | |
| NM_001291911.1:c.*111G>A | NP_001278840.1:n.*111G>A | |
| XM_017025781.1:c.*111G>A | XP_016881270.1:n.*111G>A |