gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.52117792 (AFR)
Genomes Max Group AF
0.52117792 (AFR)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.136178367A>G , CM000667.2:g.136178367A>G | GRCh38 |
| NC_000005.9:g.135514055A>G , CM000667.1:g.135514055A>G | GRCh37 |
| NC_000005.8:g.135541954A>G | NCBI36 |
| NG_032037.1:g.50521A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000545279.6:c.*887A>G MANE Select | ENSP00000441954.2:n.*887A>G | |
| ENST00000513418.1:c.164+3735A>G | ||
| ENST00000545279.5:c.*887A>G | ENSP00000441954.2:n.*887A>G | |
| ENST00000545620.5:c.*887A>G | ENSP00000446474.2:n.*887A>G | |
| NM_001001419.2:c.*887A>G | NP_001001419.1:n.*887A>G | |
| NM_001001420.2:c.*887A>G | NP_001001420.1:n.*887A>G | |
| NM_005903.6:c.*887A>G | NP_005894.3:n.*887A>G | |
| XM_017009470.2:c.*887A>G | XP_016864959.1:n.*887A>G | |
| XM_024446046.1:c.*887A>G | XP_024301814.1:n.*887A>G | |
| XM_024446047.1:c.*887A>G | XP_024301815.1:n.*887A>G | |
| NM_005903.7:c.*887A>G MANE Select | NP_005894.3:n.*887A>G | |
| NM_001001419.3:c.*887A>G | NP_001001419.1:n.*887A>G | |
| NM_001001420.3:c.*887A>G | NP_001001420.1:n.*887A>G |