Canonical Allele Identifier: CA382668892
Gene: HTR3B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113932369A>C , CM000673.2:g.113932369A>C GRCh38
NC_000011.9:g.113803091A>C , CM000673.1:g.113803091A>C GRCh37
NC_000011.8:g.113308301A>C NCBI36
NG_011483.1:g.32503A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260191.8:c.449A>C MANE Select ENSP00000260191.2:p.Gln150Pro
ENST00000260191.7:c.449A>C ENSP00000260191.2:p.Gln150Pro
ENST00000260191.6:c.449A>C ENSP00000260191.2:p.Gln150Pro
ENST00000537778.5:c.416A>C ENSP00000443118.1:p.Gln139Pro
ENST00000543092.1:c.235A>C
NM_006028.4:c.449A>C NP_006019.1:p.Gln150Pro
XM_011543063.1:c.416A>C XP_011541365.1:p.Gln139Pro
XM_011543064.1:c.248A>C XP_011541366.1:p.Gln83Pro
XM_011543065.1:c.242A>C XP_011541367.1:p.Gln81Pro
XM_011543066.1:c.416A>C XP_011541368.1:p.Gln139Pro
NM_001363563.1:c.416A>C NP_001350492.1:p.Gln139Pro
XM_017018552.2:c.242A>C XP_016874041.1:p.Gln81Pro
XM_024448767.1:c.155A>C XP_024304535.1:p.Gln52Pro
XR_001748034.2:n.700A>C
NM_001363563.2:c.416A>C NP_001350492.1:p.Gln139Pro
NM_006028.5:c.449A>C MANE Select NP_006019.1:p.Gln150Pro