Canonical Allele Identifier: CA168097932
Gene: MGAM HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs111416424
gnomAD v2: 7-141627053-T-C
gnomAD v3: 7-141927253-T-C
gnomAD v4: 7-141927253-T-C
MyVariant Identifiers: chr7:g.141627053T>C (hg19) chr7:g.141927253T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927253T>C , CM000669.2:g.141927253T>C GRCh38
NC_000007.13:g.141627053T>C , CM000669.1:g.141627053T>C GRCh37
NC_000007.12:g.141273522T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18568T>C (MGAM) ENSP00000419372.1:n.-179-18568T>C
ENST00000497554.1:n.37-2524T>C (MGAM)
XM_011515783.1:c.*24+7409T>C (OR9A4) XP_011514085.1:n.*24+7409T>C
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