Canonical Allele Identifier: CA698828746

Linked Data

dbSNP Id: rs1422083513

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50620203T>G , CM000675.2:g.50620203T>G GRCh38
NC_000013.10:g.51194339T>G , CM000675.1:g.51194339T>G GRCh37
NC_000013.9:g.50092340T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651397.1:n.1033+63703A>C (DLEU7)
ENST00000470726.6:n.347-99444T>G (DLEU1)
ENST00000479420.5:n.560-28387T>G (DLEU1)
ENST00000484869.6:n.1330-11074T>G (DLEU1)