Canonical Allele Identifier: CA1748245758

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973986T= , CM000669.2:g.141973986T= GRCh38
NC_000007.13:g.141673786T= , CM000669.1:g.141673786T= GRCh37
NC_000007.12:g.141320255T= NCBI36
NG_016141.1:g.4788A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27989T= (MGAM) ENSP00000419372.1:n.-3+27989T=
XM_011515783.1:c.*25-12410T= (OR9A4) XP_011514085.1:n.*25-12410T=