Linked Data
dbSNP Id:
rs11225434
gnomAD v2:
11-102691482-T-C
gnomAD v3:
11-102820751-T-C
gnomAD v4:
11-102820751-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102820751T>C , CM000673.2:g.102820751T>C | GRCh38 |
| NC_000011.9:g.102691482T>C , CM000673.1:g.102691482T>C | GRCh37 |
| NC_000011.8:g.102196692T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371455.7:n.424-9981T>C | ||
| ENST00000525739.6:n.683-9981T>C | ||
| ENST00000544704.1:n.444-9981T>C | ||
| NR_038390.1:n.683-9981T>C |