Canonical Allele Identifier: CA834335655
Gene: MGAM HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs1417958801
gnomAD v3: 7-141927269-A-G
gnomAD v4: 7-141927269-A-G
MyVariant Identifiers: chr7:g.141927269A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927269A>G , CM000669.2:g.141927269A>G GRCh38
NC_000007.13:g.141627069A>G , CM000669.1:g.141627069A>G GRCh37
NC_000007.12:g.141273538A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18552A>G (MGAM) ENSP00000419372.1:n.-179-18552A>G
ENST00000497554.1:n.37-2508A>G (MGAM)
XM_011515783.1:c.*24+7425A>G (OR9A4) XP_011514085.1:n.*24+7425A>G
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