Linked Data
dbSNP Id:
rs1005739087
gnomAD v3:
11-102798383-A-T
gnomAD v4:
11-102798383-A-T
MyVariant Identifiers:
chr11:g.102798383A>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102798383A>T , CM000673.2:g.102798383A>T | GRCh38 |
| NC_000011.9:g.102669114A>T , CM000673.1:g.102669114A>T | GRCh37 |
| NC_000011.8:g.102174324A>T | NCBI36 |
| NG_011740.1:g.4853T>A | |
| NG_011740.2:g.4853T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371455.7:n.423+261A>T | ||
| ENST00000525739.6:n.682+261A>T | ||
| ENST00000544704.1:n.443+261A>T | ||
| NR_038390.1:n.682+261A>T |