Linked Data
dbSNP Id:
rs1379088501
gnomAD v3:
11-14893992-C-T
gnomAD v4:
11-14893992-C-T
MyVariant Identifiers:
chr11:g.14893992C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.14893992C>T , CM000673.2:g.14893992C>T | GRCh38 |
| NC_000011.9:g.14915538C>T , CM000673.1:g.14915538C>T | GRCh37 |
| NC_000011.8:g.14872114C>T | NCBI36 |
| NG_007936.1:g.3214G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011519898.1:c.-1748G>A | XP_011518200.1:n.-1748G>A | |
| XM_011519898.3:c.-1748G>A | XP_011518200.1:n.-1748G>A |