Canonical Allele Identifier: CA2673999431
Gene: HTR1A HGNC NCBI

Linked Data

gnomAD v4: 5-63962131-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63962131C>T , CM000667.2:g.63962131C>T GRCh38
NC_000005.9:g.63257958C>T , CM000667.1:g.63257958C>T GRCh37
NC_000005.8:g.63293714C>T NCBI36
NG_032816.1:g.5162G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.-412G>A MANE Select ENSP00000316244.4:n.-412G>A
ENST00000323865.4:c.-412G>A ENSP00000316244.3:n.-412G>A
ENST00000506598.1:c.-387-25G>A ENSP00000423433.1:n.-387-25G>A
NM_000524.3:c.-412G>A NP_000515.2:n.-412G>A
NM_000524.4:c.-412G>A MANE Select NP_000515.2:n.-412G>A
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