Canonical Allele Identifier: CA1392628876
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743585A= , CM000665.2:g.109743585A= GRCh38
NC_000003.11:g.109462432A= , CM000665.1:g.109462432A= GRCh37
NC_000003.10:g.110945122A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924325.1:n.142+63390A=