Canonical Allele Identifier: CA357963642
Gene: TACR3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.104577418A>G (hg19) chr4:g.103656261A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.103656261A>G , CM000666.2:g.103656261A>G GRCh38
NC_000004.11:g.104577418A>G , CM000666.1:g.104577418A>G GRCh37
NC_000004.10:g.104796867A>G NCBI36
NG_023344.1:g.68556T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000304883.3:c.821T>C MANE Select ENSP00000303325.2:p.Leu274Pro
ENST00000304883.2:c.821T>C ENSP00000303325.2:p.Leu274Pro
NM_001059.2:c.821T>C NP_001050.1:p.Leu274Pro
NM_001059.3:c.821T>C MANE Select NP_001050.1:p.Leu274Pro
Search 100 bp 5'
Search 100 bp 3'