Canonical Allele Identifier: CA369564787
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs1803398642
MyVariant Identifiers: chr7:g.141672996C>G (hg19) chr7:g.141973196C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973196C>G , CM000669.2:g.141973196C>G GRCh38
NC_000007.13:g.141672996C>G , CM000669.1:g.141672996C>G GRCh37
NC_000007.12:g.141319465C>G NCBI36
NG_016141.1:g.5578G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27199C>G (MGAM) ENSP00000419372.1:n.-3+27199C>G
ENST00000547270.1:c.494G>C (TAS2R38) MANE Select ENSP00000448219.1:p.Arg165Thr
NM_176817.4:c.494G>C (TAS2R38) NP_789787.4:p.Arg165Thr
XM_011515783.1:c.*25-13200C>G (OR9A4) XP_011514085.1:n.*25-13200C>G
NM_176817.5:c.494G>C (TAS2R38) MANE Select NP_789787.5:p.Arg165Thr
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