Canonical Allele Identifier: CA1818161749
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127012573G= , CM000670.2:g.127012573G= GRCh38
NC_000008.10:g.128024818G= , CM000670.1:g.128024818G= GRCh37
NC_000008.9:g.128094000G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746076.2:n.1364+5955G=