Canonical Allele Identifier: CA1804794052
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269533T= , CM000670.2:g.97269533T= GRCh38
NC_000008.10:g.98281761T= , CM000670.1:g.98281761T= GRCh37
NC_000008.9:g.98350937T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125390.1:n.471+149537A=