Linked Data
ClinVar Variation Id:
259214
ClinVar RCV Id:
RCV000246955
dbSNP Id:
rs191461105
gnomAD v2:
13-20763777-C-A
gnomAD v3:
13-20189638-C-A
gnomAD v4:
13-20189638-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.20189638C>A , CM000675.2:g.20189638C>A | GRCh38 |
| NC_000013.10:g.20763777C>A , CM000675.1:g.20763777C>A | GRCh37 |
| NC_000013.9:g.19661777C>A | NCBI36 |
| NG_008358.1:g.8338G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382844.2:c.-57G>T | ENSP00000372295.1:n.-57G>T | |
| ENST00000382848.5:c.-22-35G>T MANE Select | ENSP00000372299.4:n.-22-35G>T | |
| ENST00000382844.1:c.-57G>T | ENSP00000372295.1:n.-57G>T | |
| ENST00000382848.4:c.-22-35G>T | ENSP00000372299.4:n.-22-35G>T | |
| NM_004004.5:c.-22-35G>T | NP_003995.2:n.-22-35G>T | |
| XM_011535049.1:c.-22-35G>T | XP_011533351.1:n.-22-35G>T | |
| XM_011535049.2:c.-22-35G>T | XP_011533351.1:n.-22-35G>T | |
| NM_004004.6:c.-22-35G>T MANE Select | NP_003995.2:n.-22-35G>T |