Canonical Allele Identifier: CA3031032
Gene: TACR3 HGNC NCBI

Linked Data

dbSNP Id: rs373465053
ExAC: 4:104577325 G / T
gnomAD v2: 4-104577325-G-T
gnomAD v4: 4-103656168-G-T
MyVariant Identifiers: chr4:g.104577325G>T (hg19) chr4:g.103656168G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.103656168G>T , CM000666.2:g.103656168G>T GRCh38
NC_000004.11:g.104577325G>T , CM000666.1:g.104577325G>T GRCh37
NC_000004.10:g.104796774G>T NCBI36
NG_023344.1:g.68649C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000304883.3:c.888+26C>A MANE Select ENSP00000303325.2:n.888+26C>A
ENST00000304883.2:c.888+26C>A ENSP00000303325.2:n.888+26C>A
NM_001059.2:c.888+26C>A NP_001050.1:n.888+26C>A
NM_001059.3:c.888+26C>A MANE Select NP_001050.1:n.888+26C>A
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