Linked Data
dbSNP Id:
rs1799636742
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150851846C>T , CM000669.2:g.150851846C>T | GRCh38 |
| NC_000007.13:g.150548934C>T , CM000669.1:g.150548934C>T | GRCh37 |
| NC_000007.12:g.150179867C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000467291.5:c.-92-269C>T | ENSP00000418328.1:n.-92-269C>T | |
| ENST00000493429.5:c.-92-269C>T | ENSP00000418614.1:n.-92-269C>T | |
| XM_011516008.1:c.-181-269C>T | XP_011514310.1:n.-181-269C>T | |
| XM_011516009.1:c.-92-269C>T | XP_011514311.1:n.-92-269C>T | |
| XR_928169.1:n.296-10401G>A | ||
| XR_928170.1:n.426-10401G>A | ||
| XR_928171.1:n.298-10401G>A | ||
| XM_017011944.1:c.-92-269C>T | XP_016867433.1:n.-92-269C>T | |
| XM_017011945.1:c.-92-269C>T | XP_016867434.1:n.-92-269C>T | |
| XR_928169.2:n.302-10401G>A | ||
| XR_928171.2:n.302-10401G>A |