Linked Data
dbSNP Id:
rs10794288
gnomAD v3:
11-1086825-C-T
gnomAD v4:
11-1086825-C-T
MyVariant Identifiers:
chr11:g.1086825C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.1086825C>T , CM000673.2:g.1086825C>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000361558.7:n.2643C>T | ||
| ENST00000675028.1:c.2616C>T | ENSP00000502432.1:p.Asp872= | |
| NM_002457.3:c.2616C>T | NP_002448.3:p.Asp872= |