Canonical Allele Identifier: CA2685283399

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972612G>A , CM000669.2:g.141972612G>A GRCh38
NC_000007.13:g.141672412G>A , CM000669.1:g.141672412G>A GRCh37
NC_000007.12:g.141318881G>A NCBI36
NG_016141.1:g.6162C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+26615G>A (MGAM) ENSP00000419372.1:n.-3+26615G>A
XM_011515783.1:c.*25-13784G>A (OR9A4) XP_011514085.1:n.*25-13784G>A