Canonical Allele Identifier: CA2685280212

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927291C>A , CM000669.2:g.141927291C>A GRCh38
NC_000007.13:g.141627091C>A , CM000669.1:g.141627091C>A GRCh37
NC_000007.12:g.141273560C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18530C>A (MGAM) ENSP00000419372.1:n.-179-18530C>A
ENST00000497554.1:n.37-2486C>A (MGAM)
XM_011515783.1:c.*24+7447C>A (OR9A4) XP_011514085.1:n.*24+7447C>A