Canonical Allele Identifier: CA1458424514
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54072411T= , CM000666.2:g.54072411T= GRCh38
NC_000004.11:g.54938578T= , CM000666.1:g.54938578T= GRCh37
NC_000004.10:g.54633335T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000507166.5:c.1018-202514T= ENSP00000423325.1:n.1018-202514T=