gnomAD v2:
gnomAD v4:
Joint Max Group AF
0.00000875 (SAS)
Exomes Max Group AF
0.00000924 (SAS)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.173911933G>T , CM000663.2:g.173911933G>T | GRCh38 |
| NC_000001.10:g.173881071G>T , CM000663.1:g.173881071G>T | GRCh37 |
| NC_000001.9:g.172147694G>T | NCBI36 |
| NG_012462.1:g.10446C>A , LRG_577:g.10446C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367698.4:c.490C>A MANE Select | ENSP00000356671.3:p.Arg164= | |
| ENST00000367698.3:c.490C>A | ENSP00000356671.3:p.Arg164= | |
| ENST00000487183.1:n.195C>A | ||
| ENST00000617423.4:c.490C>A | ENSP00000478688.1:p.Arg164= | |
| NM_000488.3:c.490C>A , LRG_577t1:c.490C>A | NP_000479.1:p.Arg164= | |
| XM_005245198.2:c.346C>A | XP_005245255.1:p.Arg116= | |
| NM_001365052.1:c.346C>A | NP_001351981.1:p.Arg116= | |
| NM_000488.4:c.490C>A MANE Select | NP_000479.1:p.Arg164= | |
| NM_001365052.2:c.346C>A | NP_001351981.1:p.Arg116= | |
| NM_001386302.1:c.490C>A | NP_001373231.1:p.Arg164= | |
| NM_001386303.1:c.571C>A | NP_001373232.1:p.Arg191= | |
| NM_001386304.1:c.490C>A | NP_001373233.1:p.Arg164= | |
| NM_001386305.1:c.490C>A | NP_001373234.1:p.Arg164= | |
| NM_001386306.1:c.409-1042C>A | NP_001373235.1:n.409-1042C>A |