Canonical Allele Identifier: CA2685283563

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973884G>A , CM000669.2:g.141973884G>A GRCh38
NC_000007.13:g.141673684G>A , CM000669.1:g.141673684G>A GRCh37
NC_000007.12:g.141320153G>A NCBI36
NG_016141.1:g.4890C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27887G>A (MGAM) ENSP00000419372.1:n.-3+27887G>A
XM_011515783.1:c.*25-12512G>A (OR9A4) XP_011514085.1:n.*25-12512G>A