Linked Data
dbSNP Id:
rs1761992528
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3836908T>G , CM000668.2:g.3836908T>G | GRCh38 |
| NC_000006.11:g.3837142T>G , CM000668.1:g.3837142T>G | GRCh37 |
| NC_000006.10:g.3782141T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017010729.1:c.-24+4897T>G | XP_016866218.1:n.-24+4897T>G |