Canonical Allele Identifier: CA382668757

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803043A>C (hg19) ; chr11:g.113932321A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932321A>C , CM000673.2:g.113932321A>C	GRCh38
NC_000011.9:g.113803043A>C , CM000673.1:g.113803043A>C	GRCh37
NC_000011.8:g.113308253A>C	NCBI36
NG_011483.1:g.32455A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.401A>C MANE Select	ENSP00000260191.2:p.Tyr134Ser
ENST00000260191.7:c.401A>C	ENSP00000260191.2:p.Tyr134Ser
ENST00000260191.6:c.401A>C	ENSP00000260191.2:p.Tyr134Ser
ENST00000537778.5:c.368A>C	ENSP00000443118.1:p.Tyr123Ser
ENST00000543092.1:c.187A>C
NM_006028.4:c.401A>C	NP_006019.1:p.Tyr134Ser
XM_011543063.1:c.368A>C	XP_011541365.1:p.Tyr123Ser
XM_011543064.1:c.200A>C	XP_011541366.1:p.Tyr67Ser
XM_011543065.1:c.194A>C	XP_011541367.1:p.Tyr65Ser
XM_011543066.1:c.368A>C	XP_011541368.1:p.Tyr123Ser
NM_001363563.1:c.368A>C	NP_001350492.1:p.Tyr123Ser
XM_017018552.2:c.194A>C	XP_016874041.1:p.Tyr65Ser
XM_024448767.1:c.107A>C	XP_024304535.1:p.Tyr36Ser
XR_001748034.2:n.652A>C
NM_001363563.2:c.368A>C	NP_001350492.1:p.Tyr123Ser
NM_006028.5:c.401A>C MANE Select	NP_006019.1:p.Tyr134Ser