Canonical Allele Identifier: CA1748227960

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927256T= , CM000669.2:g.141927256T= GRCh38
NC_000007.13:g.141627056T= , CM000669.1:g.141627056T= GRCh37
NC_000007.12:g.141273525T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18565T= (MGAM) ENSP00000419372.1:n.-179-18565T=
ENST00000497554.1:n.37-2521T= (MGAM)
XM_011515783.1:c.*24+7412T= (OR9A4) XP_011514085.1:n.*24+7412T=