Canonical Allele Identifier: CA2267413190
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788865C= , CM000679.2:g.57788865C= GRCh38
NC_000017.10:g.55866226C= , CM000679.1:g.55866226C= GRCh37
NC_000017.9:g.53221225C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934881.1:n.1608-16669G=
XR_934881.3:n.3815-16669G=