Linked Data
ClinVar Variation Id:
42925
ClinVar RCV Id:
RCV000035815
dbSNP Id:
rs397516164
gnomAD v2:
14-23893322-C-T
gnomAD v4:
14-23424113-C-T
PubMed:
PMID:19336582
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23424113C>T , CM000676.2:g.23424113C>T | GRCh38 |
| NC_000014.8:g.23893322C>T , CM000676.1:g.23893322C>T | GRCh37 |
| NC_000014.7:g.22963162C>T | NCBI36 |
| NG_007884.1:g.16549G>A , LRG_384:g.16549G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.2716G>A MANE Select | ENSP00000347507.3:p.Asp906Asn | |
| ENST00000355349.3:c.2716G>A | ENSP00000347507.3:p.Asp906Asn | |
| NM_000257.3:c.2716G>A | NP_000248.2:p.Asp906Asn | |
| XR_245686.3:n.2822G>A | ||
| XM_017021340.1:c.2716G>A | XP_016876829.1:p.Asp906Asn | |
| NM_000257.4:c.2716G>A MANE Select | NP_000248.2:p.Asp906Asn |