Linked Data
dbSNP Id:
rs3868075
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31200038A>T , CM000668.2:g.31200038A>T | GRCh38 |
| NC_000006.11:g.31167815A>T , CM000668.1:g.31167815A>T | GRCh37 |
| NC_000006.10:g.31275794A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000383331.4:c.123+2156A>T | ||
| ENST00000414008.2:n.145A>T | ||
| ENST00000424675.1:c.44+1857A>T | ||
| NR_026791.1:n.123+2156A>T |