Canonical Allele Identifier: CA989591494
Gene:

Linked Data

dbSNP Id: rs1910119715

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477769_41477771del , CM000680.2:g.41477769_41477771del GRCh38
NC_000018.9:g.39057733_39057735del , CM000680.1:g.39057733_39057735del GRCh37
NC_000018.8:g.37311731_37311733del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935409.1:n.86-26365_86-26363del