Linked Data
dbSNP Id:
rs1651831479
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.152304730_152304731insGGC , CM000663.2:g.152304730_152304731insGGC | GRCh38 |
| NC_000001.10:g.152277206_152277207insGGC , CM000663.1:g.152277206_152277207insGGC | GRCh37 |
| NC_000001.9:g.150543830_150543831insGGC | NCBI36 |
| NG_016190.1:g.25473_25474insGCC , LRG_1028:g.25473_25474insGCC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368799.2:c.10155_10156insGCC MANE Select | ENSP00000357789.1:p.Ser3385_Phe3386insAla | |
| ENST00000368799.1:c.10155_10156insGCC | ENSP00000357789.1:p.Ser3385_Phe3386insAla | |
| NM_002016.1:c.10155_10156insGCC , LRG_1028t1:c.10155_10156insGCC | NP_002007.1:p.Ser3385_Phe3386insAla | |
| XM_011509329.1:c.9109-898_9109-897insGCC | XP_011507631.1:n.9109-898_9109-897insGCC | |
| NM_002016.2:c.10155_10156insGCC MANE Select | NP_002007.1:p.Ser3385_Phe3386insAla |