Linked Data
dbSNP Id:
rs1855809920
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.69648197dup , CM000673.2:g.69648197dup | GRCh38 |
| NC_000011.9:g.69462965dup , CM000673.1:g.69462965dup | GRCh37 |
| NC_000011.8:g.69172146dup | NCBI36 |
| NG_007375.1:g.12093dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227507.3:c.723+55dup MANE Select | ENSP00000227507.2:n.723+55dup | |
| ENST00000227507.2:c.723+55dup | ENSP00000227507.2:n.723+55dup | |
| ENST00000536559.1:c.*198dup | ENSP00000438482.1:n.*198dup | |
| ENST00000542367.1:n.186+55dup | ||
| NM_053056.2:c.723+55dup | NP_444284.1:n.723+55dup | |
| XM_006718653.2:c.747+55dup | XP_006718716.1:n.747+55dup | |
| NM_053056.3:c.723+55dup MANE Select | NP_444284.1:n.723+55dup |