Canonical Allele Identifier: CA2271197023
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240160C= , CM000679.2:g.66240160C= GRCh38
NC_000017.10:g.64236278C= , CM000679.1:g.64236278C= GRCh37
NC_000017.9:g.61666740C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10738G= ENSP00000464301.1:p.=