Canonical Allele Identifier: CA2575420771
Gene: HTR2A HGNC NCBI

Linked Data

gnomAD v4: 13-46896090-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46896090C>T , CM000675.2:g.46896090C>T GRCh38
NC_000013.10:g.47470225C>T , CM000675.1:g.47470225C>T GRCh37
NC_000013.9:g.46368226C>T NCBI36
NG_013011.1:g.5945G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.-184G>A MANE Select ENSP00000437737.1:n.-184G>A
ENST00000543956.5:c.-78+584G>A ENSP00000441861.2:n.-78+584G>A
ENST00000542664.3:c.-184G>A ENSP00000437737.1:n.-184G>A
ENST00000543956.4:c.160+584G>A ENSP00000441861.1:n.160+584G>A
NM_000621.4:c.-184G>A NP_000612.1:n.-184G>A
NM_001165947.2:c.160+584G>A NP_001159419.1:n.160+584G>A
NM_000621.5:c.-184G>A MANE Select NP_000612.1:n.-184G>A
NM_001165947.5:c.-78+584G>A NP_001159419.2:n.-78+584G>A
NM_001378924.1:c.-184G>A NP_001365853.1:n.-184G>A
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