Canonical Allele Identifier: CA171706478
Gene:

Linked Data

dbSNP Id: rs796075626

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5907550_5907551delinsCA , CM000670.2:g.5907550_5907551delinsCA GRCh38
NC_000008.10:g.5765072_5765073delinsCA , CM000670.1:g.5765072_5765073delinsCA GRCh37
NC_000008.9:g.5752480_5752481delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941374.1:n.308-7820_308-7819delinsTG
XR_941375.1:n.308-7820_308-7819delinsTG
XR_941376.1:n.406-7820_406-7819delinsTG
XR_941377.1:n.308-7820_308-7819delinsTG
XR_941378.1:n.216-7820_216-7819delinsTG
XR_001745765.1:n.308-7820_308-7819delinsTG
XR_001745766.1:n.406-7820_406-7819delinsTG
XR_001745767.1:n.216-7820_216-7819delinsTG
XR_001745768.1:n.308-7820_308-7819delinsTG
XR_941374.2:n.308-7820_308-7819delinsTG
XR_941375.2:n.308-7820_308-7819delinsTG