Canonical Allele Identifier: CA249964172

Linked Data

dbSNP Id: rs374835673

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50620286T>C , CM000675.2:g.50620286T>C GRCh38
NC_000013.10:g.51194422T>C , CM000675.1:g.51194422T>C GRCh37
NC_000013.9:g.50092423T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651397.1:n.1033+63620A>G (DLEU7)
ENST00000470726.6:n.347-99361T>C (DLEU1)
ENST00000479420.5:n.560-28304T>C (DLEU1)
ENST00000484869.6:n.1330-10991T>C (DLEU1)