Canonical Allele Identifier: CA382669028

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803118C>A (hg19) ; chr11:g.113932396C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932396C>A , CM000673.2:g.113932396C>A	GRCh38
NC_000011.9:g.113803118C>A , CM000673.1:g.113803118C>A	GRCh37
NC_000011.8:g.113308328C>A	NCBI36
NG_011483.1:g.32530C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.476C>A MANE Select	ENSP00000260191.2:p.Thr159Lys
ENST00000260191.7:c.476C>A	ENSP00000260191.2:p.Thr159Lys
ENST00000260191.6:c.476C>A	ENSP00000260191.2:p.Thr159Lys
ENST00000537778.5:c.443C>A	ENSP00000443118.1:p.Thr148Lys
ENST00000543092.1:c.262C>A
NM_006028.4:c.476C>A	NP_006019.1:p.Thr159Lys
XM_011543063.1:c.443C>A	XP_011541365.1:p.Thr148Lys
XM_011543064.1:c.275C>A	XP_011541366.1:p.Thr92Lys
XM_011543065.1:c.269C>A	XP_011541367.1:p.Thr90Lys
XM_011543066.1:c.443C>A	XP_011541368.1:p.Thr148Lys
NM_001363563.1:c.443C>A	NP_001350492.1:p.Thr148Lys
XM_017018552.2:c.269C>A	XP_016874041.1:p.Thr90Lys
XM_024448767.1:c.182C>A	XP_024304535.1:p.Thr61Lys
XR_001748034.2:n.727C>A
NM_001363563.2:c.443C>A	NP_001350492.1:p.Thr148Lys
NM_006028.5:c.476C>A MANE Select	NP_006019.1:p.Thr159Lys