Canonical Allele Identifier: CA168094837
Gene: MGAM HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs192064136 rs2115092337 rs2115092339
gnomAD v2: 7-141673650-G-A
gnomAD v3: 7-141973850-G-A
gnomAD v4: 7-141973850-G-A
MyVariant Identifiers: chr7:g.141673650G>A (hg19) chr7:g.141973850G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973850G>A , CM000669.2:g.141973850G>A GRCh38
NC_000007.13:g.141673650G>A , CM000669.1:g.141673650G>A GRCh37
NC_000007.12:g.141320119G>A NCBI36
NG_016141.1:g.4924C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27853G>A (MGAM) ENSP00000419372.1:n.-3+27853G>A
XM_011515783.1:c.*25-12546G>A (OR9A4) XP_011514085.1:n.*25-12546G>A
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