Canonical Allele Identifier: CA4520260

Gene: MGAM TAS2R38 OR9A4

Linked Data

• dbSNP Id: rs371175533
• ExAC: 7:141673435 G / A
• gnomAD v2: 7-141673435-G-A
• gnomAD v4: 7-141973635-G-A
• MyVariant Identifiers: chr7:g.141673435G>A (hg19) ; chr7:g.141973635G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.141973635G>A , CM000669.2:g.141973635G>A	GRCh38
NC_000007.13:g.141673435G>A , CM000669.1:g.141673435G>A	GRCh37
NC_000007.12:g.141319904G>A	NCBI36
NG_016141.1:g.5139C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465654.5:c.-3+27638G>A (MGAM)	ENSP00000419372.1:n.-3+27638G>A
ENST00000547270.1:c.55C>T (TAS2R38) MANE Select	ENSP00000448219.1:p.Leu19=
NM_176817.4:c.55C>T (TAS2R38)	NP_789787.4:p.Leu19=
XM_011515783.1:c.*25-12761G>A (OR9A4)	XP_011514085.1:n.*25-12761G>A
NM_176817.5:c.55C>T (TAS2R38) MANE Select	NP_789787.5:p.Leu19=