Linked Data
dbSNP Id:
rs1176628423
MyVariant Identifiers:
chr15:g.45772381_45772382insATC (hg19)
chr15:g.45480183_45480184insATC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.45480185_45480187dup , CM000677.2:g.45480185_45480187dup | GRCh38 |
| NC_000015.9:g.45772383_45772385dup , CM000677.1:g.45772383_45772385dup | GRCh37 |
| NC_000015.8:g.43559675_43559677dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261867.5:c.*4977_*4979dup MANE Select | ENSP00000261867.3:n.*4977_*4979dup | |
| ENST00000261867.4:c.*4977_*4979dup | ENSP00000261867.3:n.*4977_*4979dup | |
| NM_013309.5:c.*4977_*4979dup | NP_037441.2:n.*4977_*4979dup | |
| NM_013309.6:c.*4977_*4979dup MANE Select | NP_037441.2:n.*4977_*4979dup |