Linked Data
dbSNP Id:
rs773963041
ExAC:
3:49162730 A / G
gnomAD v2:
3-49162730-A-G
gnomAD v4:
3-49125297-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.49125297A>G , CM000665.2:g.49125297A>G | GRCh38 |
| NC_000003.11:g.49162730A>G , CM000665.1:g.49162730A>G | GRCh37 |
| NC_000003.10:g.49137734A>G | NCBI36 |
| NG_008094.1:g.12870T>C | |
| NG_054716.1:g.642T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305544.9:c.2676T>C MANE Select | ENSP00000307156.4:p.Ala892= | |
| ENST00000305544.8:c.2676T>C | ENSP00000307156.4:p.Ala892= | |
| ENST00000418109.5:c.2676T>C | ENSP00000388325.1:p.Ala892= | |
| ENST00000462930.5:n.83T>C | ||
| ENST00000464891.5:n.425T>C | ||
| ENST00000477701.1:n.549T>C | ||
| ENST00000483057.1:n.276T>C | ||
| ENST00000486298.5:n.426-128T>C | ||
| NM_002292.3:c.2676T>C | NP_002283.3:p.Ala892= | |
| XM_005265127.3:c.2676T>C | XP_005265184.1:p.Ala892= | |
| XM_005265127.4:c.2676T>C | XP_005265184.1:p.Ala892= | |
| NM_002292.4:c.2676T>C MANE Select | NP_002283.3:p.Ala892= |