Canonical Allele Identifier: CA1796404089
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.79191180G= , CM000670.2:g.79191180G= GRCh38
NC_000008.10:g.80103415G= , CM000670.1:g.80103415G= GRCh37
NC_000008.9:g.80265970G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745720.1:n.105+809G=