Canonical Allele Identifier: CA1392628899
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743636G= , CM000665.2:g.109743636G= GRCh38
NC_000003.11:g.109462483G= , CM000665.1:g.109462483G= GRCh37
NC_000003.10:g.110945173G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924325.1:n.142+63441G=