Linked Data
dbSNP Id:
rs771029079
ExAC:
1:94884021 G / A
gnomAD v2:
1-94884021-G-A
gnomAD v3:
1-94418465-G-A
gnomAD v4:
1-94418465-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94418465G>A , CM000663.2:g.94418465G>A | GRCh38 |
| NC_000001.10:g.94884021G>A , CM000663.1:g.94884021G>A | GRCh37 |
| NC_000001.9:g.94656609G>A | NCBI36 |
| NG_008865.1:g.5089G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370214.9:c.-14G>A MANE Select | ENSP00000359233.4:n.-14G>A | |
| ENST00000647998.2:c.-14G>A | ENSP00000497921.2:n.-14G>A | |
| ENST00000370214.8:c.-14G>A | ENSP00000359233.4:n.-14G>A | |
| NM_001122674.1:c.-14G>A | NP_001116146.1:n.-14G>A | |
| NM_002858.3:c.-14G>A | NP_002849.1:n.-14G>A | |
| XM_006710802.2:c.-14G>A | XP_006710865.2:n.-14G>A | |
| NM_002858.4:c.-14G>A MANE Select | NP_002849.1:n.-14G>A | |
| NM_001122674.2:c.-14G>A | NP_001116146.1:n.-14G>A |