Canonical Allele Identifier: CA601784374
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs1443414471
gnomAD v2: 11-113774152-T-G
gnomAD v3: 11-113903430-T-G
gnomAD v4: 11-113903430-T-G
MyVariant Identifiers: chr11:g.113774152T>G (hg19) chr11:g.113903430T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903430T>G , CM000673.2:g.113903430T>G GRCh38
NC_000011.9:g.113774152T>G , CM000673.1:g.113774152T>G GRCh37
NC_000011.8:g.113279362T>G NCBI36
NG_011483.1:g.3564T>G

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4347T>G XP_011541366.1:n.12+4347T>G
XM_024448767.1:c.-243+4347T>G XP_024304535.1:n.-243+4347T>G
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