Canonical Allele Identifier: CA1804794296
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269702G= , CM000670.2:g.97269702G= GRCh38
NC_000008.10:g.98281930G= , CM000670.1:g.98281930G= GRCh37
NC_000008.9:g.98351106G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149368C=