Linked Data
dbSNP Id:
rs1967974625
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6713840_6713841insG , CM000681.2:g.6713840_6713841insG | GRCh38 |
| NC_000019.9:g.6713851_6713852insG , CM000681.1:g.6713851_6713852insG | GRCh37 |
| NC_000019.8:g.6664851_6664852insG | NCBI36 |
| NG_009557.1:g.11811_11812insC , LRG_27:g.11811_11812insC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.650+151_650+152insC | ENSP00000512083.1:n.650+151_650+152insC | |
| ENST00000245907.11:c.773+151_773+152insC MANE Select | ENSP00000245907.4:n.773+151_773+152insC | |
| ENST00000245907.10:c.773+151_773+152insC | ENSP00000245907.4:n.773+151_773+152insC | |
| ENST00000595577.1:n.277+151_277+152insC | ||
| NM_000064.3:c.773+151_773+152insC | NP_000055.2:n.773+151_773+152insC | |
| NM_000064.4:c.773+151_773+152insC MANE Select | NP_000055.2:n.773+151_773+152insC |