Linked Data
dbSNP Id:
rs2092066785
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.105766103C>A , CM000676.2:g.105766103C>A | GRCh38 |
| NC_000014.8:g.106232440C>A , CM000676.1:g.106232440C>A | GRCh37 |
| NC_000014.7:g.105303485C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641136.1:c.1257-106G>T |