Canonical Allele Identifier: CA168097953

Linked Data

dbSNP Id: rs782740822

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927282A>T , CM000669.2:g.141927282A>T GRCh38
NC_000007.13:g.141627082A>T , CM000669.1:g.141627082A>T GRCh37
NC_000007.12:g.141273551A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18539A>T (MGAM) ENSP00000419372.1:n.-179-18539A>T
ENST00000497554.1:n.37-2495A>T (MGAM)
XM_011515783.1:c.*24+7438A>T (OR9A4) XP_011514085.1:n.*24+7438A>T