Canonical Allele Identifier: CA168097955

Gene: MGAM OR9A4

Linked Data

• dbSNP Id: rs551464728
• gnomAD v3: 7-141927299-T-C
• gnomAD v4: 7-141927299-T-C
• MyVariant Identifiers: chr7:g.141627099T>C (hg19) ; chr7:g.141927299T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.141927299T>C , CM000669.2:g.141927299T>C	GRCh38
NC_000007.13:g.141627099T>C , CM000669.1:g.141627099T>C	GRCh37
NC_000007.12:g.141273568T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000465654.5:c.-179-18522T>C (MGAM)	ENSP00000419372.1:n.-179-18522T>C
ENST00000497554.1:n.37-2478T>C (MGAM)
XM_011515783.1:c.*24+7455T>C (OR9A4)	XP_011514085.1:n.*24+7455T>C