Canonical Allele Identifier: CA10616847
Gene: TACR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 347102
ClinVar RCV Id: RCV000384433
dbSNP Id: rs886058970
MyVariant Identifiers: chr4:g.104510637C>G (hg19) chr4:g.103589480C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.103589480C>G , CM000666.2:g.103589480C>G GRCh38
NC_000004.11:g.104510637C>G , CM000666.1:g.104510637C>G GRCh37
NC_000004.10:g.104730086C>G NCBI36
NG_023344.1:g.135337G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000304883.3:c.*202G>C MANE Select ENSP00000303325.2:n.*202G>C
ENST00000304883.2:c.*202G>C ENSP00000303325.2:n.*202G>C
NM_001059.2:c.*202G>C NP_001050.1:n.*202G>C
NM_001059.3:c.*202G>C MANE Select NP_001050.1:n.*202G>C
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