Canonical Allele Identifier: CA369564802
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

gnomAD v4: 7-141973202-A-G
MyVariant Identifiers: chr7:g.141673002A>G (hg19) chr7:g.141973202A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973202A>G , CM000669.2:g.141973202A>G GRCh38
NC_000007.13:g.141673002A>G , CM000669.1:g.141673002A>G GRCh37
NC_000007.12:g.141319471A>G NCBI36
NG_016141.1:g.5572T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27205A>G (MGAM) ENSP00000419372.1:n.-3+27205A>G
ENST00000547270.1:c.488T>C (TAS2R38) MANE Select ENSP00000448219.1:p.Phe163Ser
NM_176817.4:c.488T>C (TAS2R38) NP_789787.4:p.Phe163Ser
XM_011515783.1:c.*25-13194A>G (OR9A4) XP_011514085.1:n.*25-13194A>G
NM_176817.5:c.488T>C (TAS2R38) MANE Select NP_789787.5:p.Phe163Ser
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