Linked Data
dbSNP Id:
rs77240995
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3836915C>G , CM000668.2:g.3836915C>G | GRCh38 |
| NC_000006.11:g.3837149C>G , CM000668.1:g.3837149C>G | GRCh37 |
| NC_000006.10:g.3782148C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017010729.1:c.-24+4904C>G | XP_016866218.1:n.-24+4904C>G |