ClinVar Variation:
dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00015939 (NFE)
Genomes Max Group AF
0.00017122 (NFE)
Exomes Max Group AF
0.00015382 (NFE)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.64753958C>T , CM000673.2:g.64753958C>T | GRCh38 |
| NC_000011.9:g.64521430C>T , CM000673.1:g.64521430C>T | GRCh37 |
| NC_000011.8:g.64278006C>T | NCBI36 |
| NG_013018.1:g.11758G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000164139.4:c.1160G>A MANE Select | ENSP00000164139.3:p.Arg387His | |
| ENST00000164139.3:c.1160G>A | ENSP00000164139.3:p.Arg387His | |
| ENST00000377432.7:c.896G>A | ENSP00000366650.3:p.Arg299His | |
| ENST00000460413.1:n.237G>A | ||
| NM_001164716.1:c.896G>A | NP_001158188.1:p.Arg299His | |
| NM_005609.2:c.1160G>A | NP_005600.1:p.Arg387His | |
| NM_005609.3:c.1160G>A | NP_005600.1:p.Arg387His | |
| NM_005609.4:c.1160G>A MANE Select | NP_005600.1:p.Arg387His |