Canonical Allele Identifier: CA103195070
Gene: TACR3 HGNC NCBI

Linked Data

dbSNP Id: rs758989173
gnomAD v3: 4-103656185-G-A
gnomAD v4: 4-103656185-G-A
MyVariant Identifiers: chr4:g.104577342G>A (hg19) chr4:g.103656185G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.103656185G>A , CM000666.2:g.103656185G>A GRCh38
NC_000004.11:g.104577342G>A , CM000666.1:g.104577342G>A GRCh37
NC_000004.10:g.104796791G>A NCBI36
NG_023344.1:g.68632C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000304883.3:c.888+9C>T MANE Select ENSP00000303325.2:n.888+9C>T
ENST00000304883.2:c.888+9C>T ENSP00000303325.2:n.888+9C>T
NM_001059.2:c.888+9C>T NP_001050.1:n.888+9C>T
NM_001059.3:c.888+9C>T MANE Select NP_001050.1:n.888+9C>T
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