Canonical Allele Identifier: CA382669058

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803124C>G (hg19) ; chr11:g.113932402C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932402C>G , CM000673.2:g.113932402C>G	GRCh38
NC_000011.9:g.113803124C>G , CM000673.1:g.113803124C>G	GRCh37
NC_000011.8:g.113308334C>G	NCBI36
NG_011483.1:g.32536C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.482C>G MANE Select	ENSP00000260191.2:p.Ala161Gly
ENST00000260191.7:c.482C>G	ENSP00000260191.2:p.Ala161Gly
ENST00000260191.6:c.482C>G	ENSP00000260191.2:p.Ala161Gly
ENST00000537778.5:c.449C>G	ENSP00000443118.1:p.Ala150Gly
ENST00000543092.1:c.268C>G
NM_006028.4:c.482C>G	NP_006019.1:p.Ala161Gly
XM_011543063.1:c.449C>G	XP_011541365.1:p.Ala150Gly
XM_011543064.1:c.281C>G	XP_011541366.1:p.Ala94Gly
XM_011543065.1:c.275C>G	XP_011541367.1:p.Ala92Gly
XM_011543066.1:c.449C>G	XP_011541368.1:p.Ala150Gly
NM_001363563.1:c.449C>G	NP_001350492.1:p.Ala150Gly
XM_017018552.2:c.275C>G	XP_016874041.1:p.Ala92Gly
XM_024448767.1:c.188C>G	XP_024304535.1:p.Ala63Gly
XR_001748034.2:n.733C>G
NM_001363563.2:c.449C>G	NP_001350492.1:p.Ala150Gly
NM_006028.5:c.482C>G MANE Select	NP_006019.1:p.Ala161Gly