Canonical Allele Identifier: CA2089311814
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1951102069
gnomAD v4: 13-46896081-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46896081C>G , CM000675.2:g.46896081C>G GRCh38
NC_000013.10:g.47470216C>G , CM000675.1:g.47470216C>G GRCh37
NC_000013.9:g.46368217C>G NCBI36
NG_013011.1:g.5954G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.-175G>C MANE Select ENSP00000437737.1:n.-175G>C
ENST00000543956.5:c.-78+593G>C ENSP00000441861.2:n.-78+593G>C
ENST00000542664.3:c.-175G>C ENSP00000437737.1:n.-175G>C
ENST00000543956.4:c.160+593G>C ENSP00000441861.1:n.160+593G>C
NM_000621.4:c.-175G>C NP_000612.1:n.-175G>C
NM_001165947.2:c.160+593G>C NP_001159419.1:n.160+593G>C
NM_000621.5:c.-175G>C MANE Select NP_000612.1:n.-175G>C
NM_001165947.5:c.-78+593G>C NP_001159419.2:n.-78+593G>C
NM_001378924.1:c.-175G>C NP_001365853.1:n.-175G>C
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