Canonical Allele Identifier: CA1804794119
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269561G= , CM000670.2:g.97269561G= GRCh38
NC_000008.10:g.98281789G= , CM000670.1:g.98281789G= GRCh37
NC_000008.9:g.98350965G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125390.1:n.471+149509C=