Canonical Allele Identifier: CA382668850

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803079A>C (hg19) ; chr11:g.113932357A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932357A>C , CM000673.2:g.113932357A>C	GRCh38
NC_000011.9:g.113803079A>C , CM000673.1:g.113803079A>C	GRCh37
NC_000011.8:g.113308289A>C	NCBI36
NG_011483.1:g.32491A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.437A>C MANE Select	ENSP00000260191.2:p.Tyr146Ser
ENST00000260191.7:c.437A>C	ENSP00000260191.2:p.Tyr146Ser
ENST00000260191.6:c.437A>C	ENSP00000260191.2:p.Tyr146Ser
ENST00000537778.5:c.404A>C	ENSP00000443118.1:p.Tyr135Ser
ENST00000543092.1:c.223A>C
NM_006028.4:c.437A>C	NP_006019.1:p.Tyr146Ser
XM_011543063.1:c.404A>C	XP_011541365.1:p.Tyr135Ser
XM_011543064.1:c.236A>C	XP_011541366.1:p.Tyr79Ser
XM_011543065.1:c.230A>C	XP_011541367.1:p.Tyr77Ser
XM_011543066.1:c.404A>C	XP_011541368.1:p.Tyr135Ser
NM_001363563.1:c.404A>C	NP_001350492.1:p.Tyr135Ser
XM_017018552.2:c.230A>C	XP_016874041.1:p.Tyr77Ser
XM_024448767.1:c.143A>C	XP_024304535.1:p.Tyr48Ser
XR_001748034.2:n.688A>C
NM_001363563.2:c.404A>C	NP_001350492.1:p.Tyr135Ser
NM_006028.5:c.437A>C MANE Select	NP_006019.1:p.Tyr146Ser