Canonical Allele Identifier: CA2271197047
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240215T= , CM000679.2:g.66240215T= GRCh38
NC_000017.10:g.64236333T= , CM000679.1:g.64236333T= GRCh37
NC_000017.9:g.61666795T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10793A= ENSP00000464301.1:p.=