Linked Data
dbSNP Id:
rs1736091618
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186194611_186194616dup , CM000666.2:g.186194611_186194616dup | GRCh38 |
| NC_000004.11:g.187115765_187115770dup , CM000666.1:g.187115765_187115770dup | GRCh37 |
| NC_000004.10:g.187352759_187352764dup | NCBI36 |
| NG_007965.1:g.8092_8097dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378802.5:c.326_327+4dup | ||
| ENST00000378802.4:c.326_327+4dup | ||
| NM_207352.3:c.326_327+4dup | ||
| XM_005262935.2:c.326_327+4dup | ||
| XM_006714184.2:c.16_17+4dup | ||
| XM_005262935.4:c.326_327+4dup | ||
| XM_017008037.1:c.16_17+4dup | ||
| NM_207352.4:c.326_327+4dup |