Linked Data
dbSNP Id:
rs1263730312
gnomAD v3:
11-14894256-T-C
gnomAD v4:
11-14894256-T-C
MyVariant Identifiers:
chr11:g.14894256T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.14894256T>C , CM000673.2:g.14894256T>C | GRCh38 |
| NC_000011.9:g.14915802T>C , CM000673.1:g.14915802T>C | GRCh37 |
| NC_000011.8:g.14872378T>C | NCBI36 |
| NG_007936.1:g.2950A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011519898.3:c.-2012A>G | XP_011518200.1:n.-2012A>G |