Linked Data
dbSNP Id:
rs753102053
ExAC:
3:190122609 A / G
gnomAD v2:
3-190122609-A-G
gnomAD v4:
3-190404820-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190404820A>G , CM000665.2:g.190404820A>G | GRCh38 |
| NC_000003.11:g.190122609A>G , CM000665.1:g.190122609A>G | GRCh37 |
| NC_000003.10:g.191605303A>G | NCBI36 |
| NG_008149.1:g.21769A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264734.3:c.276A>G MANE Select | ENSP00000264734.3:p.Gly92= | |
| ENST00000456423.2:c.115-5083A>G | ENSP00000414136.2:n.115-5083A>G | |
| ENST00000264734.2:c.486A>G | ENSP00000264734.2:p.Gly162= | |
| ENST00000456423.1:c.325-5083A>G | ENSP00000414136.1:n.325-5083A>G | |
| ENST00000468220.1:n.468A>G | ||
| NM_006580.3:c.486A>G | NP_006571.1:p.Gly162= | |
| NM_001378492.1:c.276A>G | NP_001365421.1:p.Gly92= | |
| NM_001378493.1:c.276A>G | NP_001365422.1:p.Gly92= | |
| NM_006580.4:c.276A>G MANE Select | NP_006571.2:p.Gly92= |