Canonical Allele Identifier: CA1748245569

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973782C= , CM000669.2:g.141973782C= GRCh38
NC_000007.13:g.141673582C= , CM000669.1:g.141673582C= GRCh37
NC_000007.12:g.141320051C= NCBI36
NG_016141.1:g.4992G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27785C= (MGAM) ENSP00000419372.1:n.-3+27785C=
XM_011515783.1:c.*25-12614C= (OR9A4) XP_011514085.1:n.*25-12614C=