Canonical Allele Identifier: CA1481931302
Gene: TACR3 HGNC NCBI

Linked Data

dbSNP Id: rs1725730447

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.103656191T>C , CM000666.2:g.103656191T>C GRCh38
NC_000004.11:g.104577348T>C , CM000666.1:g.104577348T>C GRCh37
NC_000004.10:g.104796797T>C NCBI36
NG_023344.1:g.68626A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000304883.3:c.888+3A>G MANE Select ENSP00000303325.2:n.888+3A>G
ENST00000304883.2:c.888+3A>G ENSP00000303325.2:n.888+3A>G
NM_001059.2:c.888+3A>G NP_001050.1:n.888+3A>G
NM_001059.3:c.888+3A>G MANE Select NP_001050.1:n.888+3A>G