Canonical Allele Identifier: CA1804794201
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269626G= , CM000670.2:g.97269626G= GRCh38
NC_000008.10:g.98281854G= , CM000670.1:g.98281854G= GRCh37
NC_000008.9:g.98351030G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125390.1:n.471+149444C=