Canonical Allele Identifier: CA2725773
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs761864605
ExAC: 3:183778021 A / G
gnomAD v2: 3-183778021-A-G
gnomAD v4: 3-184060233-A-G
MyVariant Identifiers: chr3:g.183778021A>G (hg19) chr3:g.184060233A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060233A>G , CM000665.2:g.184060233A>G GRCh38
NC_000003.11:g.183778021A>G , CM000665.1:g.183778021A>G GRCh37
NC_000003.10:g.185260715A>G NCBI36
NG_012749.1:g.12187A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1225A>G MANE Select ENSP00000322617.1:p.Thr409Ala
ENST00000318351.1:c.1225A>G ENSP00000322617.1:p.Thr409Ala
NM_130770.2:c.1225A>G NP_570126.2:p.Thr409Ala
NM_130770.3:c.1225A>G MANE Select NP_570126.2:p.Thr409Ala
Search 100 bp 5'
Search 100 bp 3'