Linked Data
ClinVar Variation Id:
370921
ClinVar RCV Id:
RCV000409760
dbSNP Id:
rs373249212
ExAC:
3:15677196 G / T
gnomAD v2:
3-15677196-G-T
gnomAD v3:
3-15635689-G-T
gnomAD v4:
3-15635689-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.15635689G>T , CM000665.2:g.15635689G>T | GRCh38 |
| NC_000003.11:g.15677196G>T , CM000665.1:g.15677196G>T | GRCh37 |
| NC_000003.10:g.15652200G>T | NCBI36 |
| NG_008019.1:g.38942G>T | |
| NG_008019.2:g.39338G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000436193.6:c.249+1G>T | ENSP00000394277.2:n.249+1G>T | |
| ENST00000671928.2:c.249+1G>T | ENSP00000500069.2:n.249+1G>T | |
| ENST00000672892.2:c.249+1G>T | ENSP00000499944.2:n.249+1G>T | |
| ENST00000303498.10:c.249+1G>T | ENSP00000306477.6:n.249+1G>T | |
| ENST00000417015.3:c.249+1G>T | ENSP00000403775.3:n.249+1G>T | |
| ENST00000427382.2:c.249+1G>T | ENSP00000397113.2:n.249+1G>T | |
| ENST00000437172.6:c.249+1G>T | ENSP00000400995.2:n.249+1G>T | |
| ENST00000449107.7:c.249+1G>T | ENSP00000388212.2:n.249+1G>T | |
| ENST00000467027.6:n.1088+1G>T | ||
| ENST00000482824.2:c.249+1G>T | ENSP00000494864.1:n.249+1G>T | |
| ENST00000643237.3:c.249+1G>T MANE Select | ENSP00000495254.2:n.249+1G>T | |
| ENST00000646371.1:c.249+1G>T | ENSP00000495866.1:n.249+1G>T | |
| ENST00000671928.1:c.15+1G>T | ENSP00000500069.1:n.15+1G>T | |
| ENST00000672065.1:c.309+1G>T | ENSP00000500403.1:n.309+1G>T | |
| ENST00000672112.1:c.315+1G>T | ENSP00000500193.1:n.315+1G>T | |
| ENST00000672141.1:c.249+1G>T | ENSP00000500210.1:n.249+1G>T | |
| ENST00000672336.1:c.249+1G>T | ENSP00000500267.1:n.249+1G>T | |
| ENST00000672427.1:c.249+1G>T | ENSP00000500131.1:n.249+1G>T | |
| ENST00000672760.1:c.249+1G>T | ENSP00000500530.1:n.249+1G>T | |
| ENST00000672892.1:c.27+1G>T | ENSP00000499944.1:n.27+1G>T | |
| ENST00000673467.1:c.249+1G>T | ENSP00000500288.1:n.249+1G>T | |
| ENST00000673620.1:c.249+1G>T | ENSP00000500325.1:n.249+1G>T | |
| ENST00000303498.9:c.309+1G>T | ENSP00000306477.5:n.309+1G>T | |
| ENST00000383778.5:c.249+1G>T | ENSP00000373288.4:n.249+1G>T | |
| ENST00000436193.5:c.249+1G>T | ENSP00000394277.1:n.249+1G>T | |
| ENST00000437172.5:c.315+1G>T | ENSP00000400995.1:n.315+1G>T | |
| ENST00000449107.5:c.315+1G>T | ENSP00000388212.1:n.315+1G>T | |
| ENST00000482824.1:n.384+1G>T | ||
| NM_000060.3:c.309+1G>T | NP_000051.1:n.309+1G>T | |
| NM_001281723.1:c.315+1G>T | NP_001268652.1:n.315+1G>T | |
| NM_001281724.1:c.315+1G>T | NP_001268653.1:n.315+1G>T | |
| NM_001281725.1:c.249+1G>T | NP_001268654.1:n.249+1G>T | |
| NM_001281726.1:c.309+1G>T | NP_001268655.1:n.309+1G>T | |
| XM_006713314.2:c.249+1G>T | XP_006713377.1:n.249+1G>T | |
| XM_011534041.1:c.249+1G>T | XP_011532343.1:n.249+1G>T | |
| NM_000060.4:c.309+1G>T | NP_000051.1:n.309+1G>T | |
| NM_001281723.2:c.315+1G>T | NP_001268652.1:n.315+1G>T | |
| NM_001281724.2:c.315+1G>T | NP_001268653.1:n.315+1G>T | |
| NM_001281725.2:c.249+1G>T | NP_001268654.1:n.249+1G>T | |
| NM_001323582.1:c.249+1G>T | NP_001310511.1:n.249+1G>T | |
| XM_011534041.2:c.249+1G>T | XP_011532343.1:n.249+1G>T | |
| XM_017007088.1:c.249+1G>T | XP_016862577.1:n.249+1G>T | |
| XM_024453724.1:c.249+1G>T | XP_024309492.1:n.249+1G>T | |
| NM_001281723.3:c.249+1G>T | NP_001268652.2:n.249+1G>T | |
| NM_001281724.3:c.249+1G>T | NP_001268653.2:n.249+1G>T | |
| NM_001370658.1:c.249+1G>T MANE Select | NP_001357587.1:n.249+1G>T | |
| NM_001370752.1:c.249+1G>T | NP_001357681.1:n.249+1G>T | |
| NM_001370753.1:c.249+1G>T | NP_001357682.1:n.249+1G>T | |
| NM_001281726.2:c.249+1G>T | NP_001268655.2:n.249+1G>T |