Linked Data
dbSNP Id:
rs567195672
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102837450T>A , CM000672.2:g.102837450T>A | GRCh38 |
| NC_000010.10:g.104597207T>A , CM000672.1:g.104597207T>A | GRCh37 |
| NC_000010.9:g.104587197T>A | NCBI36 |
| NG_007955.1:g.5084A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000638190.1:c.-89A>T | ENSP00000492539.1:n.-89A>T | |
| ENST00000638971.1:c.-89A>T | ENSP00000492313.1:n.-89A>T | |
| ENST00000369887.3:c.-89A>T | ENSP00000358903.3:n.-89A>T | |
| NM_000102.3:c.-89A>T | NP_000093.1:n.-89A>T |