Linked Data
dbSNP Id:
rs897217588
gnomAD v3:
4-177442570-C-T
gnomAD v4:
4-177442570-C-T
MyVariant Identifiers:
chr4:g.177442570C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.177442570C>T , CM000666.2:g.177442570C>T | GRCh38 |
| NC_000004.11:g.178363724C>T , CM000666.1:g.178363724C>T | GRCh37 |
| NC_000004.10:g.178600718C>T | NCBI36 |
| NG_011845.2:g.4934G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001741929.1:n.71C>T |