Linked Data
dbSNP Id:
rs1398879157
gnomAD v2:
1-173878840-C-A
gnomAD v3:
1-173909702-C-A
gnomAD v4:
1-173909702-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.173909702C>A , CM000663.2:g.173909702C>A | GRCh38 |
| NC_000001.10:g.173878840C>A , CM000663.1:g.173878840C>A | GRCh37 |
| NC_000001.9:g.172145463C>A | NCBI36 |
| NG_012462.1:g.12677G>T , LRG_577:g.12677G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367698.4:c.1003G>T MANE Select | ENSP00000356671.3:p.Val335Leu | |
| ENST00000367698.3:c.1003G>T | ENSP00000356671.3:p.Val335Leu | |
| ENST00000617423.4:c.559+2162G>T | ENSP00000478688.1:n.559+2162G>T | |
| NM_000488.3:c.1003G>T , LRG_577t1:c.1003G>T | NP_000479.1:p.Val335Leu | |
| XM_005245198.2:c.859G>T | XP_005245255.1:p.Val287Leu | |
| NM_001365052.1:c.859G>T | NP_001351981.1:p.Val287Leu | |
| NM_000488.4:c.1003G>T MANE Select | NP_000479.1:p.Val335Leu | |
| NM_001365052.2:c.859G>T | NP_001351981.1:p.Val287Leu | |
| NM_001386302.1:c.1126G>T | NP_001373231.1:p.Val376Leu | |
| NM_001386303.1:c.1084G>T | NP_001373232.1:p.Val362Leu | |
| NM_001386304.1:c.982G>T | NP_001373233.1:p.Val328Leu | |
| NM_001386305.1:c.946G>T | NP_001373234.1:p.Val316Leu | |
| NM_001386306.1:c.787G>T | NP_001373235.1:p.Val263Leu |