Canonical Allele Identifier: CA2001400116

Gene: HTR3B

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113936885G>C , CM000673.2:g.113936885G>C	GRCh38
NC_000011.9:g.113807607G>C , CM000673.1:g.113807607G>C	GRCh37
NC_000011.8:g.113312817G>C	NCBI36
NG_011483.1:g.37019G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.696+3792G>C MANE Select	ENSP00000260191.2:n.696+3792G>C
ENST00000260191.7:c.696+3792G>C	ENSP00000260191.2:n.696+3792G>C
ENST00000260191.6:c.696+3792G>C	ENSP00000260191.2:n.696+3792G>C
ENST00000537778.5:c.663+3792G>C	ENSP00000443118.1:n.663+3792G>C
ENST00000543092.1:c.482+3792G>C
NM_006028.4:c.696+3792G>C	NP_006019.1:n.696+3792G>C
XM_011543063.1:c.663+3792G>C	XP_011541365.1:n.663+3792G>C
XM_011543064.1:c.495+3792G>C	XP_011541366.1:n.495+3792G>C
XM_011543065.1:c.489+3792G>C	XP_011541367.1:n.489+3792G>C
XM_011543066.1:c.663+3792G>C	XP_011541368.1:n.663+3792G>C
NM_001363563.1:c.663+3792G>C	NP_001350492.1:n.663+3792G>C
XM_017018552.2:c.489+3792G>C	XP_016874041.1:n.489+3792G>C
XM_024448767.1:c.402+3792G>C	XP_024304535.1:n.402+3792G>C
XR_001748034.2:n.947+3792G>C
NM_001363563.2:c.663+3792G>C	NP_001350492.1:n.663+3792G>C
NM_006028.5:c.696+3792G>C MANE Select	NP_006019.1:n.696+3792G>C