Canonical Allele Identifier: CA834312602
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs1209998509
gnomAD v3: 7-141972635-T-C
gnomAD v4: 7-141972635-T-C
MyVariant Identifiers: chr7:g.141972635T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972635T>C , CM000669.2:g.141972635T>C GRCh38
NC_000007.13:g.141672435T>C , CM000669.1:g.141672435T>C GRCh37
NC_000007.12:g.141318904T>C NCBI36
NG_016141.1:g.6139A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+26638T>C (MGAM) ENSP00000419372.1:n.-3+26638T>C
ENST00000547270.1:c.*53A>G (TAS2R38) MANE Select ENSP00000448219.1:n.*53A>G
NM_176817.4:c.*53A>G (TAS2R38) NP_789787.4:n.*53A>G
XM_011515783.1:c.*25-13761T>C (OR9A4) XP_011514085.1:n.*25-13761T>C
NM_176817.5:c.*53A>G (TAS2R38) MANE Select NP_789787.5:n.*53A>G
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