Canonical Allele Identifier: CA1458424471
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54072350C= , CM000666.2:g.54072350C= GRCh38
NC_000004.11:g.54938517C= , CM000666.1:g.54938517C= GRCh37
NC_000004.10:g.54633274C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000507166.5:c.1018-202575C= ENSP00000423325.1:n.1018-202575C=