Canonical Allele Identifier: CA1062621860
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54072288C>A , CM000666.2:g.54072288C>A GRCh38
NC_000004.11:g.54938455C>A , CM000666.1:g.54938455C>A GRCh37
NC_000004.10:g.54633212C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000507166.5:c.1018-202637C>A ENSP00000423325.1:n.1018-202637C>A