Linked Data
dbSNP Id:
rs1804974465
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.63039125T>A , CM000670.2:g.63039125T>A | GRCh38 |
| NC_000008.10:g.63951684T>A , CM000670.1:g.63951684T>A | GRCh37 |
| NC_000008.9:g.64114238T>A | NCBI36 |
| NG_028126.1:g.4927A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000677327.1:n.283A>T | ||
| ENST00000679326.1:c.-357A>T | ENSP00000504262.1:n.-357A>T | |
| ENST00000260118.6:c.-357A>T | ENSP00000260118.6:n.-357A>T | |
| XM_011517623.1:c.-357A>T | XP_011515925.1:n.-357A>T |