Canonical Allele Identifier: CA834339497
Gene: MGAM HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs1418851425
MyVariant Identifiers: chr7:g.141973986T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973986T>G , CM000669.2:g.141973986T>G GRCh38
NC_000007.13:g.141673786T>G , CM000669.1:g.141673786T>G GRCh37
NC_000007.12:g.141320255T>G NCBI36
NG_016141.1:g.4788A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27989T>G (MGAM) ENSP00000419372.1:n.-3+27989T>G
XM_011515783.1:c.*25-12410T>G (OR9A4) XP_011514085.1:n.*25-12410T>G
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