Canonical Allele Identifier: CA1748245785

Linked Data

dbSNP Id: rs1803416203

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141974018T>C , CM000669.2:g.141974018T>C GRCh38
NC_000007.13:g.141673818T>C , CM000669.1:g.141673818T>C GRCh37
NC_000007.12:g.141320287T>C NCBI36
NG_016141.1:g.4756A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+28021T>C (MGAM) ENSP00000419372.1:n.-3+28021T>C
XM_011515783.1:c.*25-12378T>C (OR9A4) XP_011514085.1:n.*25-12378T>C