Canonical Allele Identifier: CA1748227964

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927260T= , CM000669.2:g.141927260T= GRCh38
NC_000007.13:g.141627060T= , CM000669.1:g.141627060T= GRCh37
NC_000007.12:g.141273529T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18561T= (MGAM) ENSP00000419372.1:n.-179-18561T=
ENST00000497554.1:n.37-2517T= (MGAM)
XM_011515783.1:c.*24+7416T= (OR9A4) XP_011514085.1:n.*24+7416T=