Linked Data
gnomAD v4:
3-185968866-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.185968866T>G , CM000665.2:g.185968866T>G | GRCh38 |
| NC_000003.11:g.185686655T>G , CM000665.1:g.185686655T>G | GRCh37 |
| NC_000003.10:g.187169349T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000306399.3:n.270+158T>G | ||
| ENST00000416764.5:n.349+149T>G | ||
| ENST00000422108.5:n.288+217T>G | ||
| ENST00000423298.5:n.137-2749T>G | ||
| ENST00000436375.5:n.342+158T>G | ||
| ENST00000445507.1:n.279+217T>G | ||
| NR_033752.2:n.349+149T>G | ||
| NR_151491.1:n.137-2749T>G |