Canonical Allele Identifier: CA2685280208

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927277G>T , CM000669.2:g.141927277G>T GRCh38
NC_000007.13:g.141627077G>T , CM000669.1:g.141627077G>T GRCh37
NC_000007.12:g.141273546G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18544G>T (MGAM) ENSP00000419372.1:n.-179-18544G>T
ENST00000497554.1:n.37-2500G>T (MGAM)
XM_011515783.1:c.*24+7433G>T (OR9A4) XP_011514085.1:n.*24+7433G>T