Linked Data
dbSNP Id:
rs369355395
ExAC:
3:190126063 A / C
gnomAD v2:
3-190126063-A-C
gnomAD v3:
3-190408274-A-C
gnomAD v4:
3-190408274-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190408274A>C , CM000665.2:g.190408274A>C | GRCh38 |
| NC_000003.11:g.190126063A>C , CM000665.1:g.190126063A>C | GRCh37 |
| NC_000003.10:g.191608757A>C | NCBI36 |
| NG_008149.1:g.25223A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264734.3:c.383-40A>C MANE Select | ENSP00000264734.3:n.383-40A>C | |
| ENST00000456423.2:c.115-1629A>C | ENSP00000414136.2:n.115-1629A>C | |
| ENST00000264734.2:c.593-40A>C | ENSP00000264734.2:n.593-40A>C | |
| ENST00000456423.1:c.325-1629A>C | ENSP00000414136.1:n.325-1629A>C | |
| NM_006580.3:c.593-40A>C | NP_006571.1:n.593-40A>C | |
| NM_001378492.1:c.383-40A>C | NP_001365421.1:n.383-40A>C | |
| NM_001378493.1:c.383-40A>C | NP_001365422.1:n.383-40A>C | |
| NM_006580.4:c.383-40A>C MANE Select | NP_006571.2:n.383-40A>C |