Canonical Allele Identifier: CA1748245718
Gene: MGAM HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs1803414552 rs2115240085
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973953C>T , CM000669.2:g.141973953C>T GRCh38
NC_000007.13:g.141673753C>T , CM000669.1:g.141673753C>T GRCh37
NC_000007.12:g.141320222C>T NCBI36
NG_016141.1:g.4821G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27956C>T (MGAM) ENSP00000419372.1:n.-3+27956C>T
XM_011515783.1:c.*25-12443C>T (OR9A4) XP_011514085.1:n.*25-12443C>T
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