Canonical Allele Identifier: CA2089311811
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1951102044
gnomAD v4: 13-46896078-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46896078G>C , CM000675.2:g.46896078G>C GRCh38
NC_000013.10:g.47470213G>C , CM000675.1:g.47470213G>C GRCh37
NC_000013.9:g.46368214G>C NCBI36
NG_013011.1:g.5957C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.-172C>G MANE Select ENSP00000437737.1:n.-172C>G
ENST00000543956.5:c.-78+596C>G ENSP00000441861.2:n.-78+596C>G
ENST00000542664.3:c.-172C>G ENSP00000437737.1:n.-172C>G
ENST00000543956.4:c.160+596C>G ENSP00000441861.1:n.160+596C>G
NM_000621.4:c.-172C>G NP_000612.1:n.-172C>G
NM_001165947.2:c.160+596C>G NP_001159419.1:n.160+596C>G
NM_000621.5:c.-172C>G MANE Select NP_000612.1:n.-172C>G
NM_001165947.5:c.-78+596C>G NP_001159419.2:n.-78+596C>G
NM_001378924.1:c.-172C>G NP_001365853.1:n.-172C>G
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