Canonical Allele Identifier: CA168093390
Gene: MGAM HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs533484258 rs2115239937
gnomAD v2: 7-141672414-A-G
gnomAD v3: 7-141972614-A-G
gnomAD v4: 7-141972614-A-G
MyVariant Identifiers: chr7:g.141672414A>G (hg19) chr7:g.141972614A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972614A>G , CM000669.2:g.141972614A>G GRCh38
NC_000007.13:g.141672414A>G , CM000669.1:g.141672414A>G GRCh37
NC_000007.12:g.141318883A>G NCBI36
NG_016141.1:g.6160T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+26617A>G (MGAM) ENSP00000419372.1:n.-3+26617A>G
XM_011515783.1:c.*25-13782A>G (OR9A4) XP_011514085.1:n.*25-13782A>G
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