Linked Data
dbSNP Id:
rs1400665799
gnomAD v2:
4-175027552-C-A
gnomAD v3:
4-174106401-C-A
gnomAD v4:
4-174106401-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.174106401C>A , CM000666.2:g.174106401C>A | GRCh38 |
| NC_000004.11:g.175027552C>A , CM000666.1:g.175027552C>A | GRCh37 |
| NC_000004.10:g.175264127C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_125896.1:n.276-8572G>T | ||
| XR_939484.1:n.877+18762C>A | ||
| XR_939485.1:n.877+18762C>A |