Canonical Allele Identifier: CA1818161775
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127012605G= , CM000670.2:g.127012605G= GRCh38
NC_000008.10:g.128024850G= , CM000670.1:g.128024850G= GRCh37
NC_000008.9:g.128094032G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746076.2:n.1364+5987G=