Canonical Allele Identifier: CA2580606861
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63506395C>A , CM000679.2:g.63506395C>A GRCh38
NC_000017.10:g.61583756C>A , CM000679.1:g.61583756C>A GRCh37
NC_000017.9:g.58937488C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1970-661C>A ENSP00000464149.1:n.1970-661C>A