Canonical Allele Identifier: CA1458424536
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54072447A= , CM000666.2:g.54072447A= GRCh38
NC_000004.11:g.54938614A= , CM000666.1:g.54938614A= GRCh37
NC_000004.10:g.54633371A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000507166.5:c.1018-202478A= ENSP00000423325.1:n.1018-202478A=