Canonical Allele Identifier: CA168097954
Gene: MGAM HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs116032721
gnomAD v2: 7-141627085-G-A
gnomAD v3: 7-141927285-G-A
gnomAD v4: 7-141927285-G-A
MyVariant Identifiers: chr7:g.141627085G>A (hg19) chr7:g.141927285G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927285G>A , CM000669.2:g.141927285G>A GRCh38
NC_000007.13:g.141627085G>A , CM000669.1:g.141627085G>A GRCh37
NC_000007.12:g.141273554G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18536G>A (MGAM) ENSP00000419372.1:n.-179-18536G>A
ENST00000497554.1:n.37-2492G>A (MGAM)
XM_011515783.1:c.*24+7441G>A (OR9A4) XP_011514085.1:n.*24+7441G>A
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