Canonical Allele Identifier: CA168093959
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs969634864
MyVariant Identifiers: chr7:g.141672833G>C (hg19) chr7:g.141973033G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973033G>C , CM000669.2:g.141973033G>C GRCh38
NC_000007.13:g.141672833G>C , CM000669.1:g.141672833G>C GRCh37
NC_000007.12:g.141319302G>C NCBI36
NG_016141.1:g.5741C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27036G>C (MGAM) ENSP00000419372.1:n.-3+27036G>C
ENST00000547270.1:c.657C>G (TAS2R38) MANE Select ENSP00000448219.1:p.Ser219=
NM_176817.4:c.657C>G (TAS2R38) NP_789787.4:p.Ser219=
XM_011515783.1:c.*25-13363G>C (OR9A4) XP_011514085.1:n.*25-13363G>C
NM_176817.5:c.657C>G (TAS2R38) MANE Select NP_789787.5:p.Ser219=
Search 100 bp 5'
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