Canonical Allele Identifier: CA1748228042

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927350G= , CM000669.2:g.141927350G= GRCh38
NC_000007.13:g.141627150G= , CM000669.1:g.141627150G= GRCh37
NC_000007.12:g.141273619G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18471G= (MGAM) ENSP00000419372.1:n.-179-18471G=
ENST00000497554.1:n.37-2427G= (MGAM)
XM_011515783.1:c.*24+7506G= (OR9A4) XP_011514085.1:n.*24+7506G=