Linked Data
ClinVar Variation Id:
1127849
ClinVar RCV Id:
RCV001460405
dbSNP Id:
rs748156710
ExAC:
1:43396303 G / A
gnomAD v2:
1-43396303-G-A
gnomAD v3:
1-42930632-G-A
gnomAD v4:
1-42930632-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.42930632G>A , CM000663.2:g.42930632G>A | GRCh38 |
| NC_000001.10:g.43396303G>A , CM000663.1:g.43396303G>A | GRCh37 |
| NC_000001.9:g.43168890G>A | NCBI36 |
| NG_008232.1:g.33545C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000426263.10:c.510C>T MANE Select | ENSP00000416293.2:p.Ile170= | |
| ENST00000674765.1:c.510C>T | ENSP00000501811.1:p.Ile170= | |
| ENST00000675112.1:n.533C>T | ||
| ENST00000676254.1:n.959C>T | ||
| ENST00000426263.7:c.510C>T | ENSP00000416293.2:p.Ile170= | |
| ENST00000439722.2:c.389C>T | ENSP00000395521.2:n.389C>T | |
| ENST00000475162.3:c.409C>T | ||
| ENST00000625233.2:n.718C>T | ||
| ENST00000630287.2:c.510C>T | ENSP00000486694.1:p.Ile170= | |
| NM_006516.2:c.510C>T | NP_006507.2:p.Ile170= | |
| NM_006516.3:c.510C>T | NP_006507.2:p.Ile170= | |
| NM_006516.4:c.510C>T MANE Select | NP_006507.2:p.Ile170= |