Canonical Allele Identifier: CA440645250
Gene: TACR3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.104577426T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.103656269T>G , CM000666.2:g.103656269T>G GRCh38
NC_000004.11:g.104577426T>G , CM000666.1:g.104577426T>G GRCh37
NC_000004.10:g.104796875T>G NCBI36
NG_023344.1:g.68548A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000304883.3:c.813A>C MANE Select ENSP00000303325.2:p.Gly271=
ENST00000304883.2:c.813A>C ENSP00000303325.2:p.Gly271=
NM_001059.2:c.813A>C NP_001050.1:p.Gly271=
NM_001059.3:c.813A>C MANE Select NP_001050.1:p.Gly271=