Canonical Allele Identifier: CA985616819
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240258C>T , CM000679.2:g.66240258C>T GRCh38
NC_000017.10:g.64236376C>T , CM000679.1:g.64236376C>T GRCh37
NC_000017.9:g.61666838C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10836G>A ENSP00000464301.1:p.=