Canonical Allele Identifier: CA12620709
Gene: MGAM HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs114673657 rs2115240134
gnomAD v2: 7-141673808-C-G
gnomAD v3: 7-141974008-C-G
gnomAD v4: 7-141974008-C-G
MyVariant Identifiers: chr7:g.141673808C>G (hg19) chr7:g.141974008C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141974008C>G , CM000669.2:g.141974008C>G GRCh38
NC_000007.13:g.141673808C>G , CM000669.1:g.141673808C>G GRCh37
NC_000007.12:g.141320277C>G NCBI36
NG_016141.1:g.4766G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+28011C>G (MGAM) ENSP00000419372.1:n.-3+28011C>G
XM_011515783.1:c.*25-12388C>G (OR9A4) XP_011514085.1:n.*25-12388C>G
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