Canonical Allele Identifier: CA1458424542
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54072459T= , CM000666.2:g.54072459T= GRCh38
NC_000004.11:g.54938626T= , CM000666.1:g.54938626T= GRCh37
NC_000004.10:g.54633383T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000507166.5:c.1018-202466T= ENSP00000423325.1:n.1018-202466T=