Canonical Allele Identifier: CA2271197058
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240240G= , CM000679.2:g.66240240G= GRCh38
NC_000017.10:g.64236358G= , CM000679.1:g.64236358G= GRCh37
NC_000017.9:g.61666820G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10818C= ENSP00000464301.1:p.=