Canonical Allele Identifier: CA369564372
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs1803394678
MyVariant Identifiers: chr7:g.141672810A>G (hg19) chr7:g.141973010A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973010A>G , CM000669.2:g.141973010A>G GRCh38
NC_000007.13:g.141672810A>G , CM000669.1:g.141672810A>G GRCh37
NC_000007.12:g.141319279A>G NCBI36
NG_016141.1:g.5764T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27013A>G (MGAM) ENSP00000419372.1:n.-3+27013A>G
ENST00000547270.1:c.680T>C (TAS2R38) MANE Select ENSP00000448219.1:p.Met227Thr
NM_176817.4:c.680T>C (TAS2R38) NP_789787.4:p.Met227Thr
XM_011515783.1:c.*25-13386A>G (OR9A4) XP_011514085.1:n.*25-13386A>G
NM_176817.5:c.680T>C (TAS2R38) MANE Select NP_789787.5:p.Met227Thr
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