Linked Data
dbSNP Id:
rs1762921027
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.135894949dup , CM000667.2:g.135894949dup | GRCh38 |
| NC_000005.9:g.135230638dup , CM000667.1:g.135230638dup | GRCh37 |
| NC_000005.8:g.135258537dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274520.2:c.183+494dup MANE Select | ENSP00000274520.1:n.183+494dup | |
| ENST00000274520.1:c.183+494dup | ENSP00000274520.1:n.183+494dup | |
| NM_000590.1:c.183+494dup | NP_000581.1:n.183+494dup | |
| NM_000590.2:c.183+494dup MANE Select | NP_000581.1:n.183+494dup |