Canonical Allele Identifier: CA1748245776

Linked Data

dbSNP Id: rs551184769

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141974001G>T , CM000669.2:g.141974001G>T GRCh38
NC_000007.13:g.141673801G>T , CM000669.1:g.141673801G>T GRCh37
NC_000007.12:g.141320270G>T NCBI36
NG_016141.1:g.4773C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+28004G>T (MGAM) ENSP00000419372.1:n.-3+28004G>T
XM_011515783.1:c.*25-12395G>T (OR9A4) XP_011514085.1:n.*25-12395G>T