Canonical Allele Identifier: CA440645247
Gene: TACR3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.104577423A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.103656266A>G , CM000666.2:g.103656266A>G GRCh38
NC_000004.11:g.104577423A>G , CM000666.1:g.104577423A>G GRCh37
NC_000004.10:g.104796872A>G NCBI36
NG_023344.1:g.68551T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000304883.3:c.816T>C MANE Select ENSP00000303325.2:p.Ile272=
ENST00000304883.2:c.816T>C ENSP00000303325.2:p.Ile272=
NM_001059.2:c.816T>C NP_001050.1:p.Ile272=
NM_001059.3:c.816T>C MANE Select NP_001050.1:p.Ile272=