Linked Data
gnomAD v4:
3-190388003-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190388003C>G , CM000665.2:g.190388003C>G | GRCh38 |
| NC_000003.11:g.190105792C>G , CM000665.1:g.190105792C>G | GRCh37 |
| NC_000003.10:g.191588486C>G | NCBI36 |
| NG_008149.1:g.4952C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264734.2:c.-117C>G | ENSP00000264734.2:n.-117C>G | |
| ENST00000468220.1:n.306+13400C>G | ||
| NM_006580.3:c.-117C>G | NP_006571.1:n.-117C>G | |
| NM_001378492.1:c.-93-234C>G | NP_001365421.1:n.-93-234C>G | |
| NM_001378493.1:c.-93-234C>G | NP_001365422.1:n.-93-234C>G |