Canonical Allele Identifier: CA228695590
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs944933748
gnomAD v2: 11-113774157-T-C
gnomAD v3: 11-113903435-T-C
gnomAD v4: 11-113903435-T-C
MyVariant Identifiers: chr11:g.113774157T>C (hg19) chr11:g.113903435T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903435T>C , CM000673.2:g.113903435T>C GRCh38
NC_000011.9:g.113774157T>C , CM000673.1:g.113774157T>C GRCh37
NC_000011.8:g.113279367T>C NCBI36
NG_011483.1:g.3569T>C

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4352T>C XP_011541366.1:n.12+4352T>C
XM_024448767.1:c.-243+4352T>C XP_024304535.1:n.-243+4352T>C
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