Canonical Allele Identifier: CA440645252
Gene: TACR3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.104577429A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.103656272A>C , CM000666.2:g.103656272A>C GRCh38
NC_000004.11:g.104577429A>C , CM000666.1:g.104577429A>C GRCh37
NC_000004.10:g.104796878A>C NCBI36
NG_023344.1:g.68545T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000304883.3:c.810T>G MANE Select ENSP00000303325.2:p.Val270=
ENST00000304883.2:c.810T>G ENSP00000303325.2:p.Val270=
NM_001059.2:c.810T>G NP_001050.1:p.Val270=
NM_001059.3:c.810T>G MANE Select NP_001050.1:p.Val270=