Canonical Allele Identifier: CA12486203

Linked Data

dbSNP Id: rs1285933

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927349G>A , CM000669.2:g.141927349G>A GRCh38
NC_000007.13:g.141627149G>A , CM000669.1:g.141627149G>A GRCh37
NC_000007.12:g.141273618G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18472G>A (MGAM) ENSP00000419372.1:n.-179-18472G>A
ENST00000497554.1:n.37-2428G>A (MGAM)
XM_011515783.1:c.*24+7505G>A (OR9A4) XP_011514085.1:n.*24+7505G>A