Canonical Allele Identifier: CA2685283406

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972620G>T , CM000669.2:g.141972620G>T GRCh38
NC_000007.13:g.141672420G>T , CM000669.1:g.141672420G>T GRCh37
NC_000007.12:g.141318889G>T NCBI36
NG_016141.1:g.6154C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+26623G>T (MGAM) ENSP00000419372.1:n.-3+26623G>T
XM_011515783.1:c.*25-13776G>T (OR9A4) XP_011514085.1:n.*25-13776G>T