Canonical Allele Identifier: CA357963661
Gene: TACR3 HGNC NCBI

Linked Data

dbSNP Id: rs2110329558
MyVariant Identifiers: chr4:g.104577427C>T (hg19) chr4:g.103656270C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.103656270C>T , CM000666.2:g.103656270C>T GRCh38
NC_000004.11:g.104577427C>T , CM000666.1:g.104577427C>T GRCh37
NC_000004.10:g.104796876C>T NCBI36
NG_023344.1:g.68547G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000304883.3:c.812G>A MANE Select ENSP00000303325.2:p.Gly271Glu
ENST00000304883.2:c.812G>A ENSP00000303325.2:p.Gly271Glu
NM_001059.2:c.812G>A NP_001050.1:p.Gly271Glu
NM_001059.3:c.812G>A MANE Select NP_001050.1:p.Gly271Glu
Search 100 bp 5'
Search 100 bp 3'