Canonical Allele Identifier: CA2144473261
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68807207G= , CM000676.2:g.68807207G= GRCh38
NC_000014.8:g.69273924G= , CM000676.1:g.69273924G= GRCh37
NC_000014.7:g.68343677G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537441.1:c.673-553C= XP_011535743.1:n.673-553C=
XM_011537442.1:c.673-553C= XP_011535744.1:n.673-553C=
XM_011537443.1:c.673-553C= XP_011535745.1:n.673-553C=