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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)
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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
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