Linked Data
dbSNP Id:
rs1216572436
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.40285481G>C , CM000681.2:g.40285481G>C | GRCh38 |
| NC_000019.9:g.40791388G>C , CM000681.1:g.40791388G>C | GRCh37 |
| NC_000019.8:g.45483228G>C | NCBI36 |
| NG_012038.2:g.4878C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000578123.5:c.-118C>G | ENSP00000462022.1:n.-118C>G | |
| XM_011526620.1:c.-118C>G | XP_011524922.1:n.-118C>G |