Canonical Allele Identifier: CA1748227950

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927249C= , CM000669.2:g.141927249C= GRCh38
NC_000007.13:g.141627049C= , CM000669.1:g.141627049C= GRCh37
NC_000007.12:g.141273518C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18572C= (MGAM) ENSP00000419372.1:n.-179-18572C=
ENST00000497554.1:n.37-2528C= (MGAM)
XM_011515783.1:c.*24+7405C= (OR9A4) XP_011514085.1:n.*24+7405C=