Canonical Allele Identifier:
CA1657688852
Gene:
Linked Data
dbSNP Id:
rs1776569366
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.117450149_117450152del , CM000668.2:g.117450149_117450152del | GRCh38 |
| NC_000006.11:g.117771312_117771315del , CM000668.1:g.117771312_117771315del | GRCh37 |
| NC_000006.10:g.117878005_117878008del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000467125.1:c.547+116703_547+116706del | ENSP00000487717.1:n.547+116703_547+116706... |