Canonical Allele Identifier: CA168094894
Gene: MGAM HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs970686158
MyVariant Identifiers: chr7:g.141973976T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973976T>C , CM000669.2:g.141973976T>C GRCh38
NC_000007.13:g.141673776T>C , CM000669.1:g.141673776T>C GRCh37
NC_000007.12:g.141320245T>C NCBI36
NG_016141.1:g.4798A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27979T>C (MGAM) ENSP00000419372.1:n.-3+27979T>C
XM_011515783.1:c.*25-12420T>C (OR9A4) XP_011514085.1:n.*25-12420T>C
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