Canonical Allele Identifier: CA1108025248

Linked Data

dbSNP Id: rs1803384324

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972629G>A , CM000669.2:g.141972629G>A GRCh38
NC_000007.13:g.141672429G>A , CM000669.1:g.141672429G>A GRCh37
NC_000007.12:g.141318898G>A NCBI36
NG_016141.1:g.6145C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+26632G>A (MGAM) ENSP00000419372.1:n.-3+26632G>A
XM_011515783.1:c.*25-13767G>A (OR9A4) XP_011514085.1:n.*25-13767G>A