Linked Data
dbSNP Id:
rs1008706767
gnomAD v2:
3-43762351-C-G
gnomAD v3:
3-43720859-C-G
gnomAD v4:
3-43720859-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.43720859C>G , CM000665.2:g.43720859C>G | GRCh38 |
| NC_000003.11:g.43762351C>G , CM000665.1:g.43762351C>G | GRCh37 |
| NC_000003.10:g.43737355C>G | NCBI36 |
| NG_007090.3:g.34977C>G | |
| NG_007090.5:g.34990C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000454293.2:c.*29+2298C>G | ENSP00000412014.2:n.*29+2298C>G | |
| ENST00000463153.2:c.306+2298C>G | ||
| ENST00000644371.2:c.*2327C>G MANE Select | ENSP00000495778.1:n.*2327C>G | |
| ENST00000649763.1:c.*29+2298C>G | ENSP00000497701.1:n.*29+2298C>G | |
| ENST00000463153.1:n.309+2298C>G | ||
| NM_016006.4:c.*2327C>G | NP_057090.2:n.*2327C>G | |
| XM_011533779.1:c.*2327C>G | XP_011532081.1:n.*2327C>G | |
| XM_011533780.1:c.*2353C>G | XP_011532082.1:n.*2353C>G | |
| XR_940447.1:n.3322C>G | ||
| NM_001355186.1:c.*29+2298C>G | NP_001342115.1:n.*29+2298C>G | |
| NM_001365649.1:c.*2327C>G | NP_001352578.1:n.*2327C>G | |
| NM_001365650.1:c.*2353C>G | NP_001352579.1:n.*2353C>G | |
| NM_016006.5:c.*2327C>G | NP_057090.2:n.*2327C>G | |
| NR_158560.1:n.3388C>G | ||
| NM_001355186.2:c.*29+2298C>G | NP_001342115.1:n.*29+2298C>G | |
| NM_016006.6:c.*2327C>G MANE Select | NP_057090.2:n.*2327C>G |