Linked Data
dbSNP Id:
rs1428123342
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.185969013_185969014insA , CM000665.2:g.185969013_185969014insA | GRCh38 |
| NC_000003.11:g.185686802_185686803insA , CM000665.1:g.185686802_185686803insA | GRCh37 |
| NC_000003.10:g.187169496_187169497insA | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306399.3:n.270+305_270+306insA | ||
| ENST00000416764.5:n.349+296_349+297insA | ||
| ENST00000422108.5:n.288+364_288+365insA | ||
| ENST00000423298.5:n.137-2602_137-2601insA | ||
| ENST00000436375.5:n.342+305_342+306insA | ||
| ENST00000445507.1:n.279+364_279+365insA | ||
| NR_033752.2:n.349+296_349+297insA | ||
| NR_151491.1:n.137-2602_137-2601insA |