Canonical Allele Identifier: CA2622959636
Gene: HTR2A HGNC NCBI

Linked Data

gnomAD v4: 13-46895935-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46895935G>T , CM000675.2:g.46895935G>T GRCh38
NC_000013.10:g.47470070G>T , CM000675.1:g.47470070G>T GRCh37
NC_000013.9:g.46368071G>T NCBI36
NG_013011.1:g.6100C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.-29C>A MANE Select ENSP00000437737.1:n.-29C>A
ENST00000543956.5:c.-78+739C>A ENSP00000441861.2:n.-78+739C>A
ENST00000378688.8:c.-29C>A ENSP00000367959.3:n.-29C>A
ENST00000542664.3:c.-29C>A ENSP00000437737.1:n.-29C>A
ENST00000543956.4:c.160+739C>A ENSP00000441861.1:n.160+739C>A
NM_000621.4:c.-29C>A NP_000612.1:n.-29C>A
NM_001165947.2:c.160+739C>A NP_001159419.1:n.160+739C>A
NM_000621.5:c.-29C>A MANE Select NP_000612.1:n.-29C>A
NM_001165947.5:c.-78+739C>A NP_001159419.2:n.-78+739C>A
NM_001378924.1:c.-29C>A NP_001365853.1:n.-29C>A
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