Canonical Allele Identifier: CA228695562

Gene: HTR3B

Linked Data

• dbSNP Id: rs559589032
• gnomAD v2: 11-113774155-T-C
• gnomAD v3: 11-113903433-T-C
• gnomAD v4: 11-113903433-T-C
• MyVariant Identifiers: chr11:g.113774155T>C (hg19) ; chr11:g.113903433T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113903433T>C , CM000673.2:g.113903433T>C	GRCh38
NC_000011.9:g.113774155T>C , CM000673.1:g.113774155T>C	GRCh37
NC_000011.8:g.113279365T>C	NCBI36
NG_011483.1:g.3567T>C

Transcript Alleles

HGVS	Amino-acid Change
XM_011543064.1:c.12+4350T>C	XP_011541366.1:n.12+4350T>C
XM_024448767.1:c.-243+4350T>C	XP_024304535.1:n.-243+4350T>C