Canonical Allele Identifier: CA834335651
Gene: MGAM HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs1369778598
gnomAD v3: 7-141927260-T-G
gnomAD v4: 7-141927260-T-G
MyVariant Identifiers: chr7:g.141927260T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927260T>G , CM000669.2:g.141927260T>G GRCh38
NC_000007.13:g.141627060T>G , CM000669.1:g.141627060T>G GRCh37
NC_000007.12:g.141273529T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18561T>G (MGAM) ENSP00000419372.1:n.-179-18561T>G
ENST00000497554.1:n.37-2517T>G (MGAM)
XM_011515783.1:c.*24+7416T>G (OR9A4) XP_011514085.1:n.*24+7416T>G
Search 100 bp 5'
Search 100 bp 3'