Linked Data
dbSNP Id:
rs2150409153
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32460612T>C , CM000668.2:g.32460612T>C | GRCh38 |
| NC_000006.11:g.32428389T>C , CM000668.1:g.32428389T>C | GRCh37 |
| NC_000006.10:g.32536367T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000449413.1:n.77-525A>G |