Canonical Allele Identifier: CA249263529
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1004216889
MyVariant Identifiers: chr13:g.47471457C>G (hg19) chr13:g.46897322C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897322C>G , CM000675.2:g.46897322C>G GRCh38
NC_000013.10:g.47471457C>G , CM000675.1:g.47471457C>G GRCh37
NC_000013.9:g.46369458C>G NCBI36
NG_013011.1:g.4713G>C

Transcript Alleles

HGVS Amino-acid change
NM_001378924.1:c.-329+630G>C NP_001365853.1:n.-329+630G>C
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