Linked Data
ClinVar Variation Id:
188619
ClinVar RCV Id:
RCV000834730
dbSNP Id:
rs7155989
gnomAD v2:
14-23893034-G-A
gnomAD v3:
14-23423825-G-A
gnomAD v4:
14-23423825-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23423825G>A , CM000676.2:g.23423825G>A | GRCh38 |
| NC_000014.8:g.23893034G>A , CM000676.1:g.23893034G>A | GRCh37 |
| NC_000014.7:g.22962874G>A | NCBI36 |
| NG_007884.1:g.16837C>T , LRG_384:g.16837C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.2922+82C>T MANE Select | ENSP00000347507.3:n.2922+82C>T | |
| ENST00000355349.3:c.2922+82C>T | ENSP00000347507.3:n.2922+82C>T | |
| NM_000257.3:c.2922+82C>T | NP_000248.2:n.2922+82C>T | |
| XR_245686.3:n.3028+82C>T | ||
| XM_017021340.1:c.2922+82C>T | XP_016876829.1:n.2922+82C>T | |
| NM_000257.4:c.2922+82C>T MANE Select | NP_000248.2:n.2922+82C>T |