Canonical Allele Identifier: CA2685280232

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927351C>G , CM000669.2:g.141927351C>G GRCh38
NC_000007.13:g.141627151C>G , CM000669.1:g.141627151C>G GRCh37
NC_000007.12:g.141273620C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18470C>G (MGAM) ENSP00000419372.1:n.-179-18470C>G
ENST00000497554.1:n.37-2426C>G (MGAM)
XM_011515783.1:c.*24+7507C>G (OR9A4) XP_011514085.1:n.*24+7507C>G