Canonical Allele Identifier: CA249964168

Linked Data

dbSNP Id: rs938618904

Genomic Alleles

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

Transcript Alleles

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