Canonical Allele Identifier: CA115855
Gene: TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2904
ClinVar RCV Id: RCV000003038
dbSNP Id: rs713598
ExAC: 7:141673345 C / G
gnomAD: 7:141673345 C / G
MyVariant Identifiers: chr7:g.141673345C>G (hg19) chr7:g.141973545C>G (hg38)
Calculator
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973545C>G , CM000669.2:g.141973545C>G GRCh38
NC_000007.13:g.141673345C>G , CM000669.1:g.141673345C>G GRCh37
NC_000007.12:g.141319814C>G NCBI36
NG_016141.1:g.5229G>C

Transcript Alleles

HGVS Amino-acid change
NM_176817.4:c.145G>C (TAS2R38) NP_789787.4:p.Ala49Pro
XM_011515783.1:c.*25-12851C>G (OR9A4) XP_011514085.1:p.=
NM_176817.5:c.145G>C (TAS2R38) NP_789787.5:p.Ala49Pro
ENST00000465654.5:c.-3+27548C>G ENSP00000419372.1:p.=
ENST00000547270.1:c.145G>C ENSP00000448219.1:p.Ala49Pro
Search 100 bp 5'
Search 100 bp 3'