Linked Data
dbSNP Id:
rs879960268
MyVariant Identifiers:
chr1:g.149855999_149856000insAG (hg19)
chr1:g.149884449_149884450insAG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149884450_149884451dup , CM000663.2:g.149884450_149884451dup | GRCh38 |
| NC_000001.10:g.149856000_149856001dup , CM000663.1:g.149856000_149856001dup | GRCh37 |
| NC_000001.9:g.148122624_148122625dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369160.3:c.377+1813_377+1814dup | ENSP00000375736.2:n.377+1813_377+1814dup |