Linked Data
dbSNP Id:
rs373792855
ExAC:
20:44576405 G / A
gnomAD v2:
20-44576405-G-A
gnomAD v3:
20-45947766-G-A
gnomAD v4:
20-45947766-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.45947766G>A , CM000682.2:g.45947766G>A | GRCh38 |
| NC_000020.10:g.44576405G>A , CM000682.1:g.44576405G>A | GRCh37 |
| NC_000020.9:g.44009812G>A | NCBI36 |
| NG_029772.1:g.29429C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000372409.8:c.*11G>A MANE Select | ENSP00000361486.3:n.*11G>A | |
| ENST00000372409.7:c.*11G>A | ENSP00000361486.3:n.*11G>A | |
| ENST00000479348.2:c.1067G>A | ||
| NM_022104.3:c.*11G>A | NP_071387.1:n.*11G>A | |
| XM_011528980.1:c.*11G>A | XP_011527282.1:n.*11G>A | |
| XM_011528981.1:c.*11G>A | XP_011527283.1:n.*11G>A | |
| XM_011528982.1:c.*11G>A | XP_011527284.1:n.*11G>A | |
| XM_011528980.3:c.*11G>A | XP_011527282.1:n.*11G>A | |
| XM_011528981.3:c.*11G>A | XP_011527283.1:n.*11G>A | |
| XM_017028013.2:c.*11G>A | XP_016883502.1:n.*11G>A | |
| XM_017028014.2:c.*11G>A | XP_016883503.1:n.*11G>A | |
| NM_022104.4:c.*11G>A MANE Select | NP_071387.1:n.*11G>A |