Canonical Allele Identifier: CA168093395
Gene: MGAM HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs941103509
gnomAD v3: 7-141972618-C-A
gnomAD v4: 7-141972618-C-A
MyVariant Identifiers: chr7:g.141972618C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972618C>A , CM000669.2:g.141972618C>A GRCh38
NC_000007.13:g.141672418C>A , CM000669.1:g.141672418C>A GRCh37
NC_000007.12:g.141318887C>A NCBI36
NG_016141.1:g.6156G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+26621C>A (MGAM) ENSP00000419372.1:n.-3+26621C>A
XM_011515783.1:c.*25-13778C>A (OR9A4) XP_011514085.1:n.*25-13778C>A
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