Canonical Allele Identifier: CA168098020
Gene: MGAM HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs7780067
gnomAD v2: 7-141627150-G-T
gnomAD v3: 7-141927350-G-T
gnomAD v4: 7-141927350-G-T
MyVariant Identifiers: chr7:g.141627150G>T (hg19) chr7:g.141927350G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927350G>T , CM000669.2:g.141927350G>T GRCh38
NC_000007.13:g.141627150G>T , CM000669.1:g.141627150G>T GRCh37
NC_000007.12:g.141273619G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18471G>T (MGAM) ENSP00000419372.1:n.-179-18471G>T
ENST00000497554.1:n.37-2427G>T (MGAM)
XM_011515783.1:c.*24+7506G>T (OR9A4) XP_011514085.1:n.*24+7506G>T
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