Canonical Allele Identifier: CA369566310
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

gnomAD v4: 7-141973611-C-A
COSMIC: COSM369362
MyVariant Identifiers: chr7:g.141673411C>A (hg19) chr7:g.141973611C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973611C>A , CM000669.2:g.141973611C>A GRCh38
NC_000007.13:g.141673411C>A , CM000669.1:g.141673411C>A GRCh37
NC_000007.12:g.141319880C>A NCBI36
NG_016141.1:g.5163G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27614C>A (MGAM) ENSP00000419372.1:n.-3+27614C>A
ENST00000547270.1:c.79G>T (TAS2R38) MANE Select ENSP00000448219.1:p.Ala27Ser
NM_176817.4:c.79G>T (TAS2R38) NP_789787.4:p.Ala27Ser
XM_011515783.1:c.*25-12785C>A (OR9A4) XP_011514085.1:n.*25-12785C>A
NM_176817.5:c.79G>T (TAS2R38) MANE Select NP_789787.5:p.Ala27Ser
Search 100 bp 5'
Search 100 bp 3'