Canonical Allele Identifier: CA2271197011
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240139T= , CM000679.2:g.66240139T= GRCh38
NC_000017.10:g.64236257T= , CM000679.1:g.64236257T= GRCh37
NC_000017.9:g.61666719T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10717A= ENSP00000464301.1:p.=