Canonical Allele Identifier: CA1108033551
Gene: MGAM HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs1802325008
gnomAD v3: 7-141927293-G-C
gnomAD v4: 7-141927293-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927293G>C , CM000669.2:g.141927293G>C GRCh38
NC_000007.13:g.141627093G>C , CM000669.1:g.141627093G>C GRCh37
NC_000007.12:g.141273562G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18528G>C (MGAM) ENSP00000419372.1:n.-179-18528G>C
ENST00000497554.1:n.37-2484G>C (MGAM)
XM_011515783.1:c.*24+7449G>C (OR9A4) XP_011514085.1:n.*24+7449G>C
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