Canonical Allele Identifier: CA458161172

Gene: MGAM TAS2R38 OR9A4

Linked Data

• MyVariant Identifiers: chr7:g.141672827T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.141973027T>G , CM000669.2:g.141973027T>G	GRCh38
NC_000007.13:g.141672827T>G , CM000669.1:g.141672827T>G	GRCh37
NC_000007.12:g.141319296T>G	NCBI36
NG_016141.1:g.5747A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465654.5:c.-3+27030T>G (MGAM)	ENSP00000419372.1:n.-3+27030T>G
ENST00000547270.1:c.663A>C (TAS2R38) MANE Select	ENSP00000448219.1:p.Gly221=
NM_176817.4:c.663A>C (TAS2R38)	NP_789787.4:p.Gly221=
XM_011515783.1:c.*25-13369T>G (OR9A4)	XP_011514085.1:n.*25-13369T>G
NM_176817.5:c.663A>C (TAS2R38) MANE Select	NP_789787.5:p.Gly221=