Canonical Allele Identifier: CA834339491
Gene: MGAM HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs1387561727
gnomAD v3: 7-141973973-T-C
gnomAD v4: 7-141973973-T-C
MyVariant Identifiers: chr7:g.141973973T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973973T>C , CM000669.2:g.141973973T>C GRCh38
NC_000007.13:g.141673773T>C , CM000669.1:g.141673773T>C GRCh37
NC_000007.12:g.141320242T>C NCBI36
NG_016141.1:g.4801A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27976T>C (MGAM) ENSP00000419372.1:n.-3+27976T>C
XM_011515783.1:c.*25-12423T>C (OR9A4) XP_011514085.1:n.*25-12423T>C
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