Canonical Allele Identifier: CA1748245749

Linked Data

dbSNP Id: rs1803415311

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973974A>T , CM000669.2:g.141973974A>T GRCh38
NC_000007.13:g.141673774A>T , CM000669.1:g.141673774A>T GRCh37
NC_000007.12:g.141320243A>T NCBI36
NG_016141.1:g.4800T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27977A>T (MGAM) ENSP00000419372.1:n.-3+27977A>T
XM_011515783.1:c.*25-12422A>T (OR9A4) XP_011514085.1:n.*25-12422A>T