Canonical Allele Identifier: CA2759709421
Gene: HTR3C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060113T>G , CM000665.2:g.184060113T>G GRCh38
NC_000003.11:g.183777901T>G , CM000665.1:g.183777901T>G GRCh37
NC_000003.10:g.185260595T>G NCBI36
NG_012749.1:g.12067T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1142-37T>G MANE Select ENSP00000322617.1:n.1142-37T>G
ENST00000318351.1:c.1142-37T>G ENSP00000322617.1:n.1142-37T>G
NM_130770.2:c.1142-37T>G NP_570126.2:n.1142-37T>G
NM_130770.3:c.1142-37T>G MANE Select NP_570126.2:n.1142-37T>G
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