Linked Data
dbSNP Id:
rs1447703194
gnomAD v3:
11-14894029-G-T
gnomAD v4:
11-14894029-G-T
MyVariant Identifiers:
chr11:g.14894029G>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.14894029G>T , CM000673.2:g.14894029G>T | GRCh38 |
| NC_000011.9:g.14915575G>T , CM000673.1:g.14915575G>T | GRCh37 |
| NC_000011.8:g.14872151G>T | NCBI36 |
| NG_007936.1:g.3177C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011519898.1:c.-1785C>A | XP_011518200.1:n.-1785C>A | |
| XM_011519898.3:c.-1785C>A | XP_011518200.1:n.-1785C>A |