Canonical Allele Identifier: CA2778193728

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141974021C>T , CM000669.2:g.141974021C>T GRCh38
NC_000007.13:g.141673821C>T , CM000669.1:g.141673821C>T GRCh37
NC_000007.12:g.141320290C>T NCBI36
NG_016141.1:g.4753G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+28024C>T (MGAM) ENSP00000419372.1:n.-3+28024C>T
XM_011515783.1:c.*25-12375C>T (OR9A4) XP_011514085.1:n.*25-12375C>T