Canonical Allele Identifier: CA1748227976

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927285G= , CM000669.2:g.141927285G= GRCh38
NC_000007.13:g.141627085G= , CM000669.1:g.141627085G= GRCh37
NC_000007.12:g.141273554G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18536G= (MGAM) ENSP00000419372.1:n.-179-18536G=
ENST00000497554.1:n.37-2492G= (MGAM)
XM_011515783.1:c.*24+7441G= (OR9A4) XP_011514085.1:n.*24+7441G=