Canonical Allele Identifier: CA2673999531
Gene: HTR1A HGNC NCBI

Linked Data

gnomAD v4: 5-63962205-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63962205C>T , CM000667.2:g.63962205C>T GRCh38
NC_000005.9:g.63258032C>T , CM000667.1:g.63258032C>T GRCh37
NC_000005.8:g.63293788C>T NCBI36
NG_032816.1:g.5088G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.-486G>A MANE Select ENSP00000316244.4:n.-486G>A
ENST00000506598.1:c.-387-99G>A ENSP00000423433.1:n.-387-99G>A
NM_000524.3:c.-486G>A NP_000515.2:n.-486G>A
NM_000524.4:c.-486G>A MANE Select NP_000515.2:n.-486G>A
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