Canonical Allele Identifier: CA2740490266
Gene: HTR3C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060129G>A , CM000665.2:g.184060129G>A GRCh38
NC_000003.11:g.183777917G>A , CM000665.1:g.183777917G>A GRCh37
NC_000003.10:g.185260611G>A NCBI36
NG_012749.1:g.12083G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1142-21G>A MANE Select ENSP00000322617.1:n.1142-21G>A
ENST00000318351.1:c.1142-21G>A ENSP00000322617.1:n.1142-21G>A
NM_130770.2:c.1142-21G>A NP_570126.2:n.1142-21G>A
NM_130770.3:c.1142-21G>A MANE Select NP_570126.2:n.1142-21G>A
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