Canonical Allele Identifier: CA1359677713
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.41043887G= , CM000665.2:g.41043887G= GRCh38
NC_000003.11:g.41085378G= , CM000665.1:g.41085378G= GRCh37
NC_000003.10:g.41060382G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940768.1:n.87C=