Canonical Allele Identifier: CA2685280213

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927292T>C , CM000669.2:g.141927292T>C GRCh38
NC_000007.13:g.141627092T>C , CM000669.1:g.141627092T>C GRCh37
NC_000007.12:g.141273561T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18529T>C (MGAM) ENSP00000419372.1:n.-179-18529T>C
ENST00000497554.1:n.37-2485T>C (MGAM)
XM_011515783.1:c.*24+7448T>C (OR9A4) XP_011514085.1:n.*24+7448T>C