Canonical Allele Identifier: CA1748227972

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927282A= , CM000669.2:g.141927282A= GRCh38
NC_000007.13:g.141627082A= , CM000669.1:g.141627082A= GRCh37
NC_000007.12:g.141273551A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18539A= (MGAM) ENSP00000419372.1:n.-179-18539A=
ENST00000497554.1:n.37-2495A= (MGAM)
XM_011515783.1:c.*24+7438A= (OR9A4) XP_011514085.1:n.*24+7438A=