Linked Data
ClinVar Variation Id:
957629
ClinVar RCV Id:
RCV001230636
dbSNP Id:
rs768347248
ExAC:
12:5153469 G / T
gnomAD v2:
12-5153469-G-T
gnomAD v4:
12-5044303-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5044303G>T , CM000674.2:g.5044303G>T | GRCh38 |
| NC_000012.11:g.5153469G>T , CM000674.1:g.5153469G>T | GRCh37 |
| NC_000012.10:g.5023730G>T | NCBI36 |
| NG_012198.1:g.5385G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.156G>T MANE Select | ENSP00000252321.3:p.Lys52Asn | |
| ENST00000252321.4:c.156G>T | ENSP00000252321.3:p.Lys52Asn | |
| NM_002234.3:c.156G>T | NP_002225.2:p.Lys52Asn | |
| NM_002234.4:c.156G>T MANE Select | NP_002225.2:p.Lys52Asn |