Linked Data
dbSNP Id:
rs1025390528
gnomAD v3:
4-176666574-C-G
gnomAD v4:
4-176666574-C-G
MyVariant Identifiers:
chr4:g.176666574C>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.176666574C>G , CM000666.2:g.176666574C>G | GRCh38 |
| NC_000004.11:g.177587725C>G , CM000666.1:g.177587725C>G | GRCh37 |
| NC_000004.10:g.177824719C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939498.1:n.121-3047C>G | ||
| XR_939499.1:n.121-3047C>G | ||
| XR_939498.2:n.208-3047C>G | ||
| XR_939499.2:n.204-3047C>G |