Canonical Allele Identifier: CA168097926

Linked Data

dbSNP Id: rs748811142

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927246G>T , CM000669.2:g.141927246G>T GRCh38
NC_000007.13:g.141627046G>T , CM000669.1:g.141627046G>T GRCh37
NC_000007.12:g.141273515G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-179-18575G>T (MGAM) ENSP00000419372.1:n.-179-18575G>T
ENST00000497554.1:n.37-2531G>T (MGAM)
XM_011515783.1:c.*24+7402G>T (OR9A4) XP_011514085.1:n.*24+7402G>T