Canonical Allele Identifier: CA2575420762
Gene: HTR2A HGNC NCBI

Linked Data

gnomAD v4: 13-46895971-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46895972del , CM000675.2:g.46895972del GRCh38
NC_000013.10:g.47470107del , CM000675.1:g.47470107del GRCh37
NC_000013.9:g.46368108del NCBI36
NG_013011.1:g.6063del

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.-66del MANE Select ENSP00000437737.1:n.-66del
ENST00000543956.5:c.-78+702del ENSP00000441861.2:n.-78+702del
ENST00000378688.8:c.-66del ENSP00000367959.3:n.-66del
ENST00000542664.3:c.-66del ENSP00000437737.1:n.-66del
ENST00000543956.4:c.160+702del ENSP00000441861.1:n.160+702del
NM_000621.4:c.-66del NP_000612.1:n.-66del
NM_001165947.2:c.160+702del NP_001159419.1:n.160+702del
NM_000621.5:c.-66del MANE Select NP_000612.1:n.-66del
NM_001165947.5:c.-78+702del NP_001159419.2:n.-78+702del
NM_001378924.1:c.-66del NP_001365853.1:n.-66del
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