Canonical Allele Identifier: CA2271197016
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240144G= , CM000679.2:g.66240144G= GRCh38
NC_000017.10:g.64236262G= , CM000679.1:g.64236262G= GRCh37
NC_000017.9:g.61666724G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10722C= ENSP00000464301.1:p.=