Canonical Allele Identifier: CA130194

Gene: TACR3

Linked Data

• ClinVar Variation Id: 14026
• ClinVar RCV Id: RCV000030898 ; RCV000059783
• dbSNP Id: rs121918125
• ExAC: 4:104512672 G / A
• gnomAD v2: 4-104512672-G-A
• gnomAD v4: 4-103591515-G-A
• MyVariant Identifiers: chr4:g.104512672G>A (hg19) ; chr4:g.103591515G>A (hg38)
• PubMed: PMID:19079066

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.103591515G>A , CM000666.2:g.103591515G>A	GRCh38
NC_000004.11:g.104512672G>A , CM000666.1:g.104512672G>A	GRCh37
NC_000004.10:g.104732121G>A	NCBI36
NG_023344.1:g.133302C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304883.3:c.1057C>T MANE Select	ENSP00000303325.2:p.Pro353Ser
ENST00000304883.2:c.1057C>T	ENSP00000303325.2:p.Pro353Ser
NM_001059.2:c.1057C>T	NP_001050.1:p.Pro353Ser
NM_001059.3:c.1057C>T MANE Select	NP_001050.1:p.Pro353Ser