Canonical Allele Identifier: CA1748245595

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973809A= , CM000669.2:g.141973809A= GRCh38
NC_000007.13:g.141673609A= , CM000669.1:g.141673609A= GRCh37
NC_000007.12:g.141320078A= NCBI36
NG_016141.1:g.4965T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27812A= (MGAM) ENSP00000419372.1:n.-3+27812A=
XM_011515783.1:c.*25-12587A= (OR9A4) XP_011514085.1:n.*25-12587A=