Canonical Allele Identifier: CA168093376

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972587G>A , CM000669.2:g.141972587G>A GRCh38
NC_000007.13:g.141672387G>A , CM000669.1:g.141672387G>A GRCh37
NC_000007.12:g.141318856G>A NCBI36
NG_016141.1:g.6187C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+26590G>A (MGAM) ENSP00000419372.1:n.-3+26590G>A
XM_011515783.1:c.*25-13809G>A (OR9A4) XP_011514085.1:n.*25-13809G>A