Canonical Allele Identifier: CA6284377

Gene: HTR3A

Linked Data

• dbSNP Id: rs1985242
• ExAC: 11:113848273 A / C
• gnomAD v2: 11-113848273-A-C
• gnomAD v3: 11-113977551-A-C
• gnomAD v4: 11-113977551-A-C
• MyVariant Identifiers: chr11:g.113848273A>C (hg19) ; chr11:g.113977551A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113977551A>C , CM000673.2:g.113977551A>C	GRCh38
NC_000011.9:g.113848273A>C , CM000673.1:g.113848273A>C	GRCh37
NC_000011.8:g.113353483A>C	NCBI36
NG_013058.1:g.7477A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000504030.7:c.68-220A>C MANE Select	ENSP00000424189.2:n.68-220A>C
ENST00000299961.5:c.-4A>C	ENSP00000299961.4:n.-4A>C
ENST00000355556.6:c.86-220A>C	ENSP00000347754.2:n.86-220A>C
ENST00000375498.6:c.86-220A>C	ENSP00000364648.2:n.86-220A>C
ENST00000504030.6:c.68-220A>C	ENSP00000424189.2:n.68-220A>C
ENST00000506841.6:c.68-220A>C	ENSP00000424776.2:n.68-220A>C
ENST00000510849.5:c.68-220A>C	ENSP00000423653.1:n.68-220A>C
NM_000869.5:c.86-220A>C	NP_000860.2:n.86-220A>C
NM_001161772.2:c.-4A>C	NP_001155244.1:n.-4A>C
NM_213621.3:c.86-220A>C	NP_998786.2:n.86-220A>C
NR_046363.1:n.319-220A>C
NM_000869.6:c.68-220A>C MANE Select	NP_000860.3:n.68-220A>C
NM_213621.4:c.68-220A>C	NP_998786.3:n.68-220A>C
NM_001161772.3:c.-4A>C	NP_001155244.1:n.-4A>C
NR_046363.2:n.286-220A>C