Canonical Allele Identifier: CA2452892591
Gene: HTR2C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.114849062T>G , CM000685.2:g.114849062T>G GRCh38
NC_000023.10:g.114083625T>G , CM000685.1:g.114083625T>G GRCh37
NC_000023.9:g.113989881T>G NCBI36
NG_012082.2:g.269978T>G
NG_012082.3:g.269978T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000276198.6:c.550+859T>G MANE Select ENSP00000276198.1:n.550+859T>G
ENST00000276198.5:c.550+859T>G ENSP00000276198.1:n.550+859T>G
ENST00000371950.3:c.455+954T>G ENSP00000361018.3:n.455+954T>G
ENST00000371951.5:c.550+859T>G ENSP00000361019.1:n.550+859T>G
NM_000868.3:c.550+859T>G NP_000859.1:n.550+859T>G
NM_001256760.2:c.550+859T>G NP_001243689.1:n.550+859T>G
NM_001256761.2:c.455+954T>G NP_001243690.1:n.455+954T>G
NM_000868.4:c.550+859T>G MANE Select NP_000859.2:n.550+859T>G
NM_001256760.3:c.550+859T>G NP_001243689.2:n.550+859T>G
NM_001256761.3:c.455+954T>G NP_001243690.2:n.455+954T>G