Canonical Allele Identifier: CA6284044

Gene: HTR3B

Linked Data

• dbSNP Id: rs34550504
• ExAC: 11:113803070 T / C
• gnomAD v2: 11-113803070-T-C
• gnomAD v3: 11-113932348-T-C
• gnomAD v4: 11-113932348-T-C
• MyVariant Identifiers: chr11:g.113803070T>C (hg19) ; chr11:g.113932348T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932348T>C , CM000673.2:g.113932348T>C	GRCh38
NC_000011.9:g.113803070T>C , CM000673.1:g.113803070T>C	GRCh37
NC_000011.8:g.113308280T>C	NCBI36
NG_011483.1:g.32482T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.428T>C MANE Select	ENSP00000260191.2:p.Ile143Thr
ENST00000260191.7:c.428T>C	ENSP00000260191.2:p.Ile143Thr
ENST00000260191.6:c.428T>C	ENSP00000260191.2:p.Ile143Thr
ENST00000537778.5:c.395T>C	ENSP00000443118.1:p.Ile132Thr
ENST00000543092.1:c.214T>C
NM_006028.4:c.428T>C	NP_006019.1:p.Ile143Thr
XM_011543063.1:c.395T>C	XP_011541365.1:p.Ile132Thr
XM_011543064.1:c.227T>C	XP_011541366.1:p.Ile76Thr
XM_011543065.1:c.221T>C	XP_011541367.1:p.Ile74Thr
XM_011543066.1:c.395T>C	XP_011541368.1:p.Ile132Thr
NM_001363563.1:c.395T>C	NP_001350492.1:p.Ile132Thr
XM_017018552.2:c.221T>C	XP_016874041.1:p.Ile74Thr
XM_024448767.1:c.134T>C	XP_024304535.1:p.Ile45Thr
XR_001748034.2:n.679T>C
NM_001363563.2:c.395T>C	NP_001350492.1:p.Ile132Thr
NM_006028.5:c.428T>C MANE Select	NP_006019.1:p.Ile143Thr