Linked Data
dbSNP Id:
rs1009118914
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3836913A>C , CM000668.2:g.3836913A>C | GRCh38 |
| NC_000006.11:g.3837147A>C , CM000668.1:g.3837147A>C | GRCh37 |
| NC_000006.10:g.3782146A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017010729.1:c.-24+4902A>C | XP_016866218.1:n.-24+4902A>C |