Canonical Allele Identifier: CA382668731

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803037T>C (hg19) ; chr11:g.113932315T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932315T>C , CM000673.2:g.113932315T>C	GRCh38
NC_000011.9:g.113803037T>C , CM000673.1:g.113803037T>C	GRCh37
NC_000011.8:g.113308247T>C	NCBI36
NG_011483.1:g.32449T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.395T>C MANE Select	ENSP00000260191.2:p.Leu132Pro
ENST00000260191.7:c.395T>C	ENSP00000260191.2:p.Leu132Pro
ENST00000260191.6:c.395T>C	ENSP00000260191.2:p.Leu132Pro
ENST00000537778.5:c.362T>C	ENSP00000443118.1:p.Leu121Pro
ENST00000543092.1:c.181T>C
NM_006028.4:c.395T>C	NP_006019.1:p.Leu132Pro
XM_011543063.1:c.362T>C	XP_011541365.1:p.Leu121Pro
XM_011543064.1:c.194T>C	XP_011541366.1:p.Leu65Pro
XM_011543065.1:c.188T>C	XP_011541367.1:p.Leu63Pro
XM_011543066.1:c.362T>C	XP_011541368.1:p.Leu121Pro
NM_001363563.1:c.362T>C	NP_001350492.1:p.Leu121Pro
XM_017018552.2:c.188T>C	XP_016874041.1:p.Leu63Pro
XM_024448767.1:c.101T>C	XP_024304535.1:p.Leu34Pro
XR_001748034.2:n.646T>C
NM_001363563.2:c.362T>C	NP_001350492.1:p.Leu121Pro
NM_006028.5:c.395T>C MANE Select	NP_006019.1:p.Leu132Pro