Canonical Allele Identifier: CA578290190
Gene: MGAM HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs1179135002 rs2115240115
gnomAD v2: 7-141673790-C-T
gnomAD v3: 7-141973990-C-T
gnomAD v4: 7-141973990-C-T
MyVariant Identifiers: chr7:g.141673790C>T (hg19) chr7:g.141973990C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973990C>T , CM000669.2:g.141973990C>T GRCh38
NC_000007.13:g.141673790C>T , CM000669.1:g.141673790C>T GRCh37
NC_000007.12:g.141320259C>T NCBI36
NG_016141.1:g.4784G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27993C>T (MGAM) ENSP00000419372.1:n.-3+27993C>T
XM_011515783.1:c.*25-12406C>T (OR9A4) XP_011514085.1:n.*25-12406C>T
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