Canonical Allele Identifier: CA2725702
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs142615813
ExAC: 3:183777669 G / A
gnomAD v2: 3-183777669-G-A
gnomAD v3: 3-184059881-G-A
gnomAD v4: 3-184059881-G-A
MyVariant Identifiers: chr3:g.183777669G>A (hg19) chr3:g.184059881G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184059881G>A , CM000665.2:g.184059881G>A GRCh38
NC_000003.11:g.183777669G>A , CM000665.1:g.183777669G>A GRCh37
NC_000003.10:g.185260363G>A NCBI36
NG_012749.1:g.11835G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.979G>A MANE Select ENSP00000322617.1:p.Val327Ile
ENST00000318351.1:c.979G>A ENSP00000322617.1:p.Val327Ile
NM_130770.2:c.979G>A NP_570126.2:p.Val327Ile
NM_130770.3:c.979G>A MANE Select NP_570126.2:p.Val327Ile
Search 100 bp 5'
Search 100 bp 3'