Linked Data
dbSNP Id:
rs869297264
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55096381_55096382insG , CM000666.2:g.55096381_55096382insG | GRCh38 |
| NC_000004.11:g.55962548_55962549insG , CM000666.1:g.55962548_55962549insG | GRCh37 |
| NC_000004.10:g.55657305_55657306insG | NCBI36 |
| NG_012004.1:g.34214_34215insC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263923.5:c.2615-40_2615-39insC MANE Select | ENSP00000263923.4:n.2615-40_2615-39insC | |
| ENST00000647068.1:n.2628-40_2628-39insC | ||
| ENST00000263923.4:c.2615-40_2615-39insC | ENSP00000263923.4:n.2615-40_2615-39insC | |
| ENST00000509309.1:n.339_340insC | ||
| NM_002253.2:c.2615-40_2615-39insC | NP_002244.1:n.2615-40_2615-39insC | |
| NM_002253.3:c.2615-40_2615-39insC | NP_002244.1:n.2615-40_2615-39insC | |
| NM_002253.4:c.2615-40_2615-39insC MANE Select | NP_002244.1:n.2615-40_2615-39insC |