Linked Data
ClinVar Variation Id:
164093
dbSNP Id:
rs727503193
ExAC:
11:47361334 G / A
gnomAD v2:
11-47361334-G-A
gnomAD v3:
11-47339783-G-A
gnomAD v4:
11-47339783-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47339783G>A , CM000673.2:g.47339783G>A | GRCh38 |
| NC_000011.9:g.47361334G>A , CM000673.1:g.47361334G>A | GRCh37 |
| NC_000011.8:g.47317910G>A | NCBI36 |
| NG_007667.1:g.17920C>T , LRG_386:g.17920C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000545968.6:c.1935C>T MANE Select | ENSP00000442795.1:p.Pro645= | |
| ENST00000256993.8:c.1935C>T | ENSP00000256993.5:p.Pro645= | |
| ENST00000399249.6:c.1935C>T | ENSP00000382193.2:p.Pro645= | |
| ENST00000544791.1:c.1935C>T | ENSP00000444259.1:p.Pro645= | |
| ENST00000545968.5:c.1935C>T | ENSP00000442795.1:p.Pro645= | |
| NM_000256.3:c.1935C>T , LRG_386t1:c.1935C>T MANE Select | NP_000247.2:p.Pro645= | |
| XM_011520117.1:c.1917C>T | XP_011518419.1:p.Pro639= | |
| XM_011520118.1:c.1935C>T | XP_011518420.1:p.Pro645= |