Linked Data
ClinVar Variation Id:
731688
ClinVar RCV Id:
RCV000906682
dbSNP Id:
rs780036327
ExAC:
1:197091639 G / A
gnomAD v2:
1-197091639-G-A
gnomAD v3:
1-197122509-G-A
gnomAD v4:
1-197122509-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197122509G>A , CM000663.2:g.197122509G>A | GRCh38 |
| NC_000001.10:g.197091639G>A , CM000663.1:g.197091639G>A | GRCh37 |
| NC_000001.9:g.195358262G>A | NCBI36 |
| NG_015867.1:g.29186C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000367408.6:n.1519C>T | ||
| ENST00000367409.9:c.3477C>T MANE Select | ENSP00000356379.4:p.Asp1159= | |
| ENST00000680112.1:n.1533C>T | ||
| ENST00000680265.1:c.3477C>T | ENSP00000505384.1:p.Asp1159= | |
| ENST00000680710.1:c.3477C>T | ENSP00000506676.1:p.Asp1159= | |
| ENST00000681879.1:c.3477C>T | ENSP00000505363.1:p.Asp1159= | |
| ENST00000294732.11:c.3477C>T | ENSP00000294732.7:p.Asp1159= | |
| ENST00000367408.5:c.1227C>T | ENSP00000356378.1:p.Asp409= | |
| ENST00000367409.8:c.3477C>T | ENSP00000356379.4:p.Asp1159= | |
| ENST00000612785.1:c.562-19862C>T | ENSP00000479244.1:n.562-19862C>T | |
| NM_001206846.1:c.3477C>T | NP_001193775.1:p.Asp1159= | |
| NM_018136.4:c.3477C>T | NP_060606.3:p.Asp1159= | |
| NM_018136.5:c.3477C>T MANE Select | NP_060606.3:p.Asp1159= | |
| NM_001206846.2:c.3477C>T | NP_001193775.1:p.Asp1159= |