Canonical Allele Identifier: CA2271197030
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240173A= , CM000679.2:g.66240173A= GRCh38
NC_000017.10:g.64236291A= , CM000679.1:g.64236291A= GRCh37
NC_000017.9:g.61666753A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10751T= ENSP00000464301.1:p.=