Canonical Allele Identifier: CA553776470
Gene: TACR3 HGNC NCBI

Linked Data

dbSNP Id: rs1341713878
gnomAD v2: 4-104577340-T-G
gnomAD v3: 4-103656183-T-G
gnomAD v4: 4-103656183-T-G
MyVariant Identifiers: chr4:g.104577340T>G (hg19) chr4:g.103656183T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.103656183T>G , CM000666.2:g.103656183T>G GRCh38
NC_000004.11:g.104577340T>G , CM000666.1:g.104577340T>G GRCh37
NC_000004.10:g.104796789T>G NCBI36
NG_023344.1:g.68634A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000304883.3:c.888+11A>C MANE Select ENSP00000303325.2:n.888+11A>C
ENST00000304883.2:c.888+11A>C ENSP00000303325.2:n.888+11A>C
NM_001059.2:c.888+11A>C NP_001050.1:n.888+11A>C
NM_001059.3:c.888+11A>C MANE Select NP_001050.1:n.888+11A>C
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