Canonical Allele Identifier: CA2580767464

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927349G>C , CM000669.2:g.141927349G>C GRCh38
NC_000007.13:g.141627149G>C , CM000669.1:g.141627149G>C GRCh37
NC_000007.12:g.141273618G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18472G>C (MGAM) ENSP00000419372.1:n.-179-18472G>C
ENST00000497554.1:n.37-2428G>C (MGAM)
XM_011515783.1:c.*24+7505G>C (OR9A4) XP_011514085.1:n.*24+7505G>C