Linked Data
dbSNP Id:
rs1744964948
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.185969010G>T , CM000665.2:g.185969010G>T | GRCh38 |
| NC_000003.11:g.185686799G>T , CM000665.1:g.185686799G>T | GRCh37 |
| NC_000003.10:g.187169493G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306399.3:n.270+302G>T | ||
| ENST00000416764.5:n.349+293G>T | ||
| ENST00000422108.5:n.288+361G>T | ||
| ENST00000423298.5:n.137-2605G>T | ||
| ENST00000436375.5:n.342+302G>T | ||
| ENST00000445507.1:n.279+361G>T | ||
| NR_033752.2:n.349+293G>T | ||
| NR_151491.1:n.137-2605G>T |