Canonical Allele Identifier: CA1748245716

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973953C= , CM000669.2:g.141973953C= GRCh38
NC_000007.13:g.141673753C= , CM000669.1:g.141673753C= GRCh37
NC_000007.12:g.141320222C= NCBI36
NG_016141.1:g.4821G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27956C= (MGAM) ENSP00000419372.1:n.-3+27956C=
XM_011515783.1:c.*25-12443C= (OR9A4) XP_011514085.1:n.*25-12443C=