gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.32420996 (EAS)
Genomes Max Group AF
0.32420996 (EAS)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.46892935T>C , CM000675.2:g.46892935T>C | GRCh38 |
| NC_000013.10:g.47467070T>C , CM000675.1:g.47467070T>C | GRCh37 |
| NC_000013.9:g.46365071T>C | NCBI36 |
| NG_013011.1:g.9100A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000542664.4:c.413-345A>G MANE Select | ENSP00000437737.1:n.413-345A>G | |
| ENST00000543956.5:c.-77-345A>G | ENSP00000441861.2:n.-77-345A>G | |
| ENST00000378688.8:c.413-345A>G | ENSP00000367959.3:n.413-345A>G | |
| ENST00000542664.3:c.413-345A>G | ENSP00000437737.1:n.413-345A>G | |
| ENST00000543956.4:c.161-345A>G | ENSP00000441861.1:n.161-345A>G | |
| NM_000621.4:c.413-345A>G | NP_000612.1:n.413-345A>G | |
| NM_001165947.2:c.161-345A>G | NP_001159419.1:n.161-345A>G | |
| NM_000621.5:c.413-345A>G MANE Select | NP_000612.1:n.413-345A>G | |
| NM_001165947.5:c.-77-345A>G | NP_001159419.2:n.-77-345A>G | |
| NM_001378924.1:c.413-345A>G | NP_001365853.1:n.413-345A>G |