Canonical Allele Identifier: CA1748245772

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141974000C= , CM000669.2:g.141974000C= GRCh38
NC_000007.13:g.141673800C= , CM000669.1:g.141673800C= GRCh37
NC_000007.12:g.141320269C= NCBI36
NG_016141.1:g.4774G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+28003C= (MGAM) ENSP00000419372.1:n.-3+28003C=
XM_011515783.1:c.*25-12396C= (OR9A4) XP_011514085.1:n.*25-12396C=