Canonical Allele Identifier: CA369565005
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs782618571
MyVariant Identifiers: chr7:g.141673084C>G (hg19) chr7:g.141973284C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973284C>G , CM000669.2:g.141973284C>G GRCh38
NC_000007.13:g.141673084C>G , CM000669.1:g.141673084C>G GRCh37
NC_000007.12:g.141319553C>G NCBI36
NG_016141.1:g.5490G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27287C>G (MGAM) ENSP00000419372.1:n.-3+27287C>G
ENST00000547270.1:c.406G>C (TAS2R38) MANE Select ENSP00000448219.1:p.Val136Leu
NM_176817.4:c.406G>C (TAS2R38) NP_789787.4:p.Val136Leu
XM_011515783.1:c.*25-13112C>G (OR9A4) XP_011514085.1:n.*25-13112C>G
NM_176817.5:c.406G>C (TAS2R38) MANE Select NP_789787.5:p.Val136Leu
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