Canonical Allele Identifier: CA2388704391
Community Standard Title: NC_000021.9:g.37952931C=

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.37952931C= , CM000683.2:g.37952931C= GRCh38
NC_000021.8:g.39325234C= , CM000683.1:g.39325234C= GRCh37
NC_000021.7:g.38247104C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398948.5:c.305G= (DSCR4) ENSP00000381921.1:p.Ser102=
ENST00000645093.1:c.-27-112222G= (KCNJ6) ENSP00000493772.1:n.-27-112222G=