Canonical Allele Identifier: CA2001421714

Gene: HTR3A

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113985959G>C , CM000673.2:g.113985959G>C	GRCh38
NC_000011.9:g.113856681G>C , CM000673.1:g.113856681G>C	GRCh37
NC_000011.8:g.113361891G>C	NCBI36
NG_013058.1:g.15885G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504030.7:c.545-56G>C MANE Select	ENSP00000424189.2:n.545-56G>C
ENST00000299961.5:c.500-56G>C	ENSP00000299961.4:n.500-56G>C
ENST00000355556.6:c.563-56G>C	ENSP00000347754.2:n.563-56G>C
ENST00000375498.6:c.563-56G>C	ENSP00000364648.2:n.563-56G>C
ENST00000502622.1:n.448-56G>C
ENST00000504030.6:c.545-56G>C	ENSP00000424189.2:n.545-56G>C
ENST00000506841.6:c.545-56G>C	ENSP00000424776.2:n.545-56G>C
ENST00000510849.5:c.545-559G>C	ENSP00000423653.1:n.545-559G>C
NM_000869.5:c.563-56G>C	NP_000860.2:n.563-56G>C
NM_001161772.2:c.500-56G>C	NP_001155244.1:n.500-56G>C
NM_213621.3:c.563-56G>C	NP_998786.2:n.563-56G>C
NR_046363.1:n.796-559G>C
NM_000869.6:c.545-56G>C MANE Select	NP_000860.3:n.545-56G>C
NM_213621.4:c.545-56G>C	NP_998786.3:n.545-56G>C
NM_001161772.3:c.500-56G>C	NP_001155244.1:n.500-56G>C
NR_046363.2:n.763-559G>C