Canonical Allele Identifier: CA357963658
Gene: TACR3 HGNC NCBI

Linked Data

dbSNP Id: rs1483228039
gnomAD v2: 4-104577425-T-C
gnomAD v4: 4-103656268-T-C
MyVariant Identifiers: chr4:g.104577425T>C (hg19) chr4:g.103656268T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.103656268T>C , CM000666.2:g.103656268T>C GRCh38
NC_000004.11:g.104577425T>C , CM000666.1:g.104577425T>C GRCh37
NC_000004.10:g.104796874T>C NCBI36
NG_023344.1:g.68549A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000304883.3:c.814A>G MANE Select ENSP00000303325.2:p.Ile272Val
ENST00000304883.2:c.814A>G ENSP00000303325.2:p.Ile272Val
NM_001059.2:c.814A>G NP_001050.1:p.Ile272Val
NM_001059.3:c.814A>G MANE Select NP_001050.1:p.Ile272Val
Search 100 bp 5'
Search 100 bp 3'