Canonical Allele Identifier: CA2090971395

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50620199T= , CM000675.2:g.50620199T= GRCh38
NC_000013.10:g.51194335T= , CM000675.1:g.51194335T= GRCh37
NC_000013.9:g.50092336T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651397.1:n.1033+63707A= (DLEU7)
ENST00000470726.6:n.347-99448T= (DLEU1)
ENST00000479420.5:n.560-28391T= (DLEU1)
ENST00000484869.6:n.1330-11078T= (DLEU1)