Canonical Allele Identifier: CA2090971421

Linked Data

dbSNP Id: rs1566203775

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50620275T>C , CM000675.2:g.50620275T>C GRCh38
NC_000013.10:g.51194411T>C , CM000675.1:g.51194411T>C GRCh37
NC_000013.9:g.50092412T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651397.1:n.1033+63631A>G (DLEU7)
ENST00000470726.6:n.347-99372T>C (DLEU1)
ENST00000479420.5:n.560-28315T>C (DLEU1)
ENST00000484869.6:n.1330-11002T>C (DLEU1)