Canonical Allele Identifier: CA2452910333
Gene: HTR2C HGNC NCBI

Linked Data

dbSNP Id: rs2071352779
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.114903677G>A , CM000685.2:g.114903677G>A GRCh38
NC_000023.10:g.114138240G>A , CM000685.1:g.114138240G>A GRCh37
NC_000023.9:g.114044496G>A NCBI36
NG_012082.2:g.324593G>A
NG_012082.3:g.324593G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000276198.6:c.551-2912G>A MANE Select ENSP00000276198.1:n.551-2912G>A
ENST00000276198.5:c.551-2912G>A ENSP00000276198.1:n.551-2912G>A
ENST00000371950.3:c.456-2912G>A ENSP00000361018.3:n.456-2912G>A
ENST00000371951.5:c.551-2912G>A ENSP00000361019.1:n.551-2912G>A
NM_000868.3:c.551-2912G>A NP_000859.1:n.551-2912G>A
NM_001256760.2:c.551-2912G>A NP_001243689.1:n.551-2912G>A
NM_001256761.2:c.456-2912G>A NP_001243690.1:n.456-2912G>A
NM_000868.4:c.551-2912G>A MANE Select NP_000859.2:n.551-2912G>A
NM_001256760.3:c.551-2912G>A NP_001243689.2:n.551-2912G>A
NM_001256761.3:c.456-2912G>A NP_001243690.2:n.456-2912G>A
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