Linked Data
dbSNP Id:
rs904235705
gnomAD v4:
1-17393967-C-T
MyVariant Identifiers:
chr1:g.17393967C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17393967C>T , CM000663.2:g.17393967C>T | GRCh38 |
| NC_000001.10:g.17720463C>T , CM000663.1:g.17720463C>T | GRCh37 |
| NC_000001.9:g.17593050C>T | NCBI36 |
| NG_032943.1:g.26722C>T | |
| NG_032943.2:g.26722C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000619609.1:c.1075-8C>T MANE Select | ENSP00000483125.1:n.1075-8C>T | |
| NM_207421.4:c.1075-8C>T MANE Select | NP_997304.3:n.1075-8C>T |