Canonical Allele Identifier: CA1796404021
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.79191016G= , CM000670.2:g.79191016G= GRCh38
NC_000008.10:g.80103251G= , CM000670.1:g.80103251G= GRCh37
NC_000008.9:g.80265806G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745720.1:n.105+645G=