Canonical Allele Identifier: CA2725744
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs746490464
ExAC: 3:183777896 T / A
gnomAD v2: 3-183777896-T-A
gnomAD v3: 3-184060108-T-A
gnomAD v4: 3-184060108-T-A
MyVariant Identifiers: chr3:g.183777896T>A (hg19) chr3:g.184060108T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060108T>A , CM000665.2:g.184060108T>A GRCh38
NC_000003.11:g.183777896T>A , CM000665.1:g.183777896T>A GRCh37
NC_000003.10:g.185260590T>A NCBI36
NG_012749.1:g.12062T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1142-42T>A MANE Select ENSP00000322617.1:n.1142-42T>A
ENST00000318351.1:c.1142-42T>A ENSP00000322617.1:n.1142-42T>A
NM_130770.2:c.1142-42T>A NP_570126.2:n.1142-42T>A
NM_130770.3:c.1142-42T>A MANE Select NP_570126.2:n.1142-42T>A
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