Canonical Allele Identifier: CA2728062081
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs2138262081
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897081C>G , CM000675.2:g.46897081C>G GRCh38
NC_000013.10:g.47471216C>G , CM000675.1:g.47471216C>G GRCh37
NC_000013.9:g.46369217C>G NCBI36
NG_013011.1:g.4954G>C

Transcript Alleles

HGVS Amino-acid Change
NM_001378924.1:c.-328-847G>C NP_001365853.1:n.-328-847G>C
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