Canonical Allele Identifier: CA671975817

Gene: HTR3B

Linked Data

• dbSNP Id: rs397802872
• gnomAD v3: 11-113932655-A-ACG
• gnomAD v4: 11-113932655-A-ACG
• MyVariant Identifiers: chr11:g.113803377_113803378insCG (hg19) ; chr11:g.113932655_113932656insCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932655_113932656insCG , CM000673.2:g.113932655_113932656insCG	GRCh38
NC_000011.9:g.113803377_113803378insCG , CM000673.1:g.113803377_113803378insCG	GRCh37
NC_000011.8:g.113308587_113308588insCG	NCBI36
NG_011483.1:g.32789_32790insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.538+197_538+198insCG MANE Select	ENSP00000260191.2:n.538+197_538+198insCG
ENST00000260191.7:c.538+197_538+198insCG	ENSP00000260191.2:n.538+197_538+198insCG
ENST00000260191.6:c.538+197_538+198insCG	ENSP00000260191.2:n.538+197_538+198insCG
ENST00000537778.5:c.505+197_505+198insCG	ENSP00000443118.1:n.505+197_505+198insCG
ENST00000543092.1:c.324+197_324+198insCG
NM_006028.4:c.538+197_538+198insCG	NP_006019.1:n.538+197_538+198insCG
XM_011543063.1:c.505+197_505+198insCG	XP_011541365.1:n.505+197_505+198insCG
XM_011543064.1:c.337+197_337+198insCG	XP_011541366.1:n.337+197_337+198insCG
XM_011543065.1:c.331+197_331+198insCG	XP_011541367.1:n.331+197_331+198insCG
XM_011543066.1:c.505+197_505+198insCG	XP_011541368.1:n.505+197_505+198insCG
NM_001363563.1:c.505+197_505+198insCG	NP_001350492.1:n.505+197_505+198insCG
XM_017018552.2:c.331+197_331+198insCG	XP_016874041.1:n.331+197_331+198insCG
XM_024448767.1:c.244+197_244+198insCG	XP_024304535.1:n.244+197_244+198insCG
XR_001748034.2:n.789+197_789+198insCG
NM_001363563.2:c.505+197_505+198insCG	NP_001350492.1:n.505+197_505+198insCG
NM_006028.5:c.538+197_538+198insCG MANE Select	NP_006019.1:n.538+197_538+198insCG