Canonical Allele Identifier: CA3030909
Gene: TACR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 347106
ClinVar RCV Id: RCV000296320 RCV000916690
dbSNP Id: rs138661164
ExAC: 4:104510947 C / T
gnomAD v2: 4-104510947-C-T
gnomAD v3: 4-103589790-C-T
gnomAD v4: 4-103589790-C-T
MyVariant Identifiers: chr4:g.104510947C>T (hg19) chr4:g.103589790C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.103589790C>T , CM000666.2:g.103589790C>T GRCh38
NC_000004.11:g.104510947C>T , CM000666.1:g.104510947C>T GRCh37
NC_000004.10:g.104730396C>T NCBI36
NG_023344.1:g.135027G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000304883.3:c.1290G>A MANE Select ENSP00000303325.2:p.Thr430=
ENST00000304883.2:c.1290G>A ENSP00000303325.2:p.Thr430=
NM_001059.2:c.1290G>A NP_001050.1:p.Thr430=
NM_001059.3:c.1290G>A MANE Select NP_001050.1:p.Thr430=
Search 100 bp 5'
Search 100 bp 3'