Canonical Allele Identifier: CA553776451
Gene: TACR3 HGNC NCBI

Linked Data

dbSNP Id: rs1314539838
gnomAD v2: 4-104577317-A-G
gnomAD v3: 4-103656160-A-G
gnomAD v4: 4-103656160-A-G
MyVariant Identifiers: chr4:g.104577317A>G (hg19) chr4:g.103656160A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.103656160A>G , CM000666.2:g.103656160A>G GRCh38
NC_000004.11:g.104577317A>G , CM000666.1:g.104577317A>G GRCh37
NC_000004.10:g.104796766A>G NCBI36
NG_023344.1:g.68657T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000304883.3:c.888+34T>C MANE Select ENSP00000303325.2:n.888+34T>C
ENST00000304883.2:c.888+34T>C ENSP00000303325.2:n.888+34T>C
NM_001059.2:c.888+34T>C NP_001050.1:n.888+34T>C
NM_001059.3:c.888+34T>C MANE Select NP_001050.1:n.888+34T>C
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