Linked Data
dbSNP Id:
rs2073513168
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.66240276T>C , CM000679.2:g.66240276T>C | GRCh38 |
| NC_000017.10:g.64236394T>C , CM000679.1:g.64236394T>C | GRCh37 |
| NC_000017.9:g.61666856T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000577982.1:c.-43-10854A>G | ENSP00000464301.1:n.-43-10854A>G |