Linked Data
dbSNP Id:
rs1560822178
gnomAD v2:
4-175027520-C-T
gnomAD v3:
4-174106369-C-T
gnomAD v4:
4-174106369-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.174106369C>T , CM000666.2:g.174106369C>T | GRCh38 |
| NC_000004.11:g.175027520C>T , CM000666.1:g.175027520C>T | GRCh37 |
| NC_000004.10:g.175264095C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_125896.1:n.276-8540G>A | ||
| XR_939484.1:n.877+18730C>T | ||
| XR_939485.1:n.877+18730C>T |