Linked Data
dbSNP Id:
rs1299794595
gnomAD v3:
11-14893706-T-A
gnomAD v4:
11-14893706-T-A
MyVariant Identifiers:
chr11:g.14893706T>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.14893706T>A , CM000673.2:g.14893706T>A | GRCh38 |
| NC_000011.9:g.14915252T>A , CM000673.1:g.14915252T>A | GRCh37 |
| NC_000011.8:g.14871828T>A | NCBI36 |
| NG_007936.1:g.3500A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_011519898.1:c.-1462A>T | XP_011518200.1:n.-1462A>T | |
| XM_011519898.3:c.-1462A>T | XP_011518200.1:n.-1462A>T |