Linked Data
dbSNP Id:
rs758535416
ExAC:
1:44466423 C / T
gnomAD v2:
1-44466423-C-T
gnomAD v3:
1-44000751-C-T
gnomAD v4:
1-44000751-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.44000751C>T , CM000663.2:g.44000751C>T | GRCh38 |
| NC_000001.10:g.44466423C>T , CM000663.1:g.44466423C>T | GRCh37 |
| NC_000001.9:g.44239010C>T | NCBI36 |
| NG_050929.1:g.35742G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372310.8:c.1536+16G>A MANE Select | ENSP00000361384.4:n.1536+16G>A | |
| ENST00000673836.1:c.1536+16G>A | ENSP00000501314.1:n.1536+16G>A | |
| ENST00000357730.6:c.1593+16G>A | ENSP00000350362.2:n.1593+16G>A | |
| ENST00000360584.6:c.1755+16G>A | ENSP00000353791.2:n.1755+16G>A | |
| ENST00000372306.7:c.1624+16G>A | ENSP00000361380.3:n.1624+16G>A | |
| ENST00000372307.7:c.1341+16G>A | ENSP00000361381.3:n.1341+16G>A | |
| ENST00000372310.7:c.1536+16G>A | ENSP00000361384.3:n.1536+16G>A | |
| ENST00000475075.6:c.1203+16G>A | ENSP00000434460.1:n.1203+16G>A | |
| NM_001024845.2:c.1536+16G>A | NP_001020016.1:n.1536+16G>A | |
| NM_001261380.1:c.1548+16G>A | NP_001248309.1:n.1548+16G>A | |
| NM_006934.3:c.1593+16G>A | NP_008865.2:n.1593+16G>A | |
| NM_201649.3:c.1755+16G>A | NP_964012.2:n.1755+16G>A | |
| NR_048548.1:n.1796+16G>A | ||
| NR_048549.1:n.1519+16G>A | ||
| XM_011542017.1:c.1755+16G>A | XP_011540319.1:n.1755+16G>A | |
| NM_001328626.1:c.1203+16G>A | NP_001315555.1:n.1203+16G>A | |
| NM_001328627.1:c.1473+16G>A | NP_001315556.1:n.1473+16G>A | |
| NM_001328628.1:c.1341+16G>A | NP_001315557.1:n.1341+16G>A | |
| NM_001328629.1:c.1536+16G>A | NP_001315558.1:n.1536+16G>A | |
| NM_001328630.1:c.1203+16G>A | NP_001315559.1:n.1203+16G>A | |
| XM_011542017.2:c.1755+16G>A | XP_011540319.1:n.1755+16G>A | |
| XM_017002152.2:c.1455+16G>A | XP_016857641.1:n.1455+16G>A | |
| XM_017002153.2:c.1422+16G>A | XP_016857642.1:n.1422+16G>A | |
| XM_024449295.1:c.1341+16G>A | XP_024305063.1:n.1341+16G>A | |
| NM_001024845.3:c.1536+16G>A MANE Select | NP_001020016.1:n.1536+16G>A | |
| NM_001261380.2:c.1548+16G>A | NP_001248309.1:n.1548+16G>A | |
| NM_001328626.2:c.1203+16G>A | NP_001315555.1:n.1203+16G>A | |
| NM_001328630.2:c.1203+16G>A | NP_001315559.1:n.1203+16G>A | |
| NM_006934.4:c.1593+16G>A | NP_008865.2:n.1593+16G>A | |
| NM_201649.4:c.1755+16G>A | NP_964012.2:n.1755+16G>A | |
| NR_048548.2:n.1619+16G>A |