Canonical Allele Identifier: CA382669317

Gene: HTR3B

Linked Data

• dbSNP Id: rs1268443887
• gnomAD v2: 11-113803181-G-C
• gnomAD v3: 11-113932459-G-C
• gnomAD v4: 11-113932459-G-C
• MyVariant Identifiers: chr11:g.113803181G>C (hg19) ; chr11:g.113932459G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932459G>C , CM000673.2:g.113932459G>C	GRCh38
NC_000011.9:g.113803181G>C , CM000673.1:g.113803181G>C	GRCh37
NC_000011.8:g.113308391G>C	NCBI36
NG_011483.1:g.32593G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.538+1G>C MANE Select	ENSP00000260191.2:n.538+1G>C
ENST00000260191.7:c.538+1G>C	ENSP00000260191.2:n.538+1G>C
ENST00000260191.6:c.538+1G>C	ENSP00000260191.2:n.538+1G>C
ENST00000537778.5:c.505+1G>C	ENSP00000443118.1:n.505+1G>C
ENST00000543092.1:c.324+1G>C
NM_006028.4:c.538+1G>C	NP_006019.1:n.538+1G>C
XM_011543063.1:c.505+1G>C	XP_011541365.1:n.505+1G>C
XM_011543064.1:c.337+1G>C	XP_011541366.1:n.337+1G>C
XM_011543065.1:c.331+1G>C	XP_011541367.1:n.331+1G>C
XM_011543066.1:c.505+1G>C	XP_011541368.1:n.505+1G>C
NM_001363563.1:c.505+1G>C	NP_001350492.1:n.505+1G>C
XM_017018552.2:c.331+1G>C	XP_016874041.1:n.331+1G>C
XM_024448767.1:c.244+1G>C	XP_024304535.1:n.244+1G>C
XR_001748034.2:n.789+1G>C
NM_001363563.2:c.505+1G>C	NP_001350492.1:n.505+1G>C
NM_006028.5:c.538+1G>C MANE Select	NP_006019.1:n.538+1G>C