Canonical Allele Identifier: CA1816081168
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395751A= , CM000670.2:g.122395751A= GRCh38
NC_000008.10:g.123407990A= , CM000670.1:g.123407990A= GRCh37
NC_000008.9:g.123477171A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+3421T=
XR_928599.3:n.152+3421T=