Linked Data
dbSNP Id:
rs2129693913
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.63038857A>G , CM000670.2:g.63038857A>G | GRCh38 |
| NC_000008.10:g.63951416A>G , CM000670.1:g.63951416A>G | GRCh37 |
| NC_000008.9:g.64113970A>G | NCBI36 |
| NG_028126.1:g.5195T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000677327.1:n.551T>C | ||
| ENST00000677482.1:c.-89T>C | ENSP00000504590.1:n.-89T>C | |
| ENST00000679326.1:c.-89T>C | ENSP00000504262.1:n.-89T>C | |
| ENST00000260118.6:c.-89T>C | ENSP00000260118.6:n.-89T>C | |
| NM_003878.2:c.-89T>C | NP_003869.1:n.-89T>C | |
| XM_011517623.1:c.-89T>C | XP_011515925.1:n.-89T>C |