Canonical Allele Identifier: CA382668686

Gene: HTR3B

Linked Data

• dbSNP Id: rs1465004280
• MyVariant Identifiers: chr11:g.113803030C>G (hg19) ; chr11:g.113932308C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932308C>G , CM000673.2:g.113932308C>G	GRCh38
NC_000011.9:g.113803030C>G , CM000673.1:g.113803030C>G	GRCh37
NC_000011.8:g.113308240C>G	NCBI36
NG_011483.1:g.32442C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.388C>G MANE Select	ENSP00000260191.2:p.Pro130Ala
ENST00000260191.7:c.388C>G	ENSP00000260191.2:p.Pro130Ala
ENST00000260191.6:c.388C>G	ENSP00000260191.2:p.Pro130Ala
ENST00000537778.5:c.355C>G	ENSP00000443118.1:p.Pro119Ala
ENST00000543092.1:c.174C>G
NM_006028.4:c.388C>G	NP_006019.1:p.Pro130Ala
XM_011543063.1:c.355C>G	XP_011541365.1:p.Pro119Ala
XM_011543064.1:c.187C>G	XP_011541366.1:p.Pro63Ala
XM_011543065.1:c.181C>G	XP_011541367.1:p.Pro61Ala
XM_011543066.1:c.355C>G	XP_011541368.1:p.Pro119Ala
NM_001363563.1:c.355C>G	NP_001350492.1:p.Pro119Ala
XM_017018552.2:c.181C>G	XP_016874041.1:p.Pro61Ala
XM_024448767.1:c.94C>G	XP_024304535.1:p.Pro32Ala
XR_001748034.2:n.639C>G
NM_001363563.2:c.355C>G	NP_001350492.1:p.Pro119Ala
NM_006028.5:c.388C>G MANE Select	NP_006019.1:p.Pro130Ala