Canonical Allele Identifier: CA813046829
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1243849689
gnomAD v3: 5-63962109-A-G
gnomAD v4: 5-63962109-A-G
MyVariant Identifiers: chr5:g.63257936A>G (hg19) chr5:g.63962109A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63962109A>G , CM000667.2:g.63962109A>G GRCh38
NC_000005.9:g.63257936A>G , CM000667.1:g.63257936A>G GRCh37
NC_000005.8:g.63293692A>G NCBI36
NG_032816.1:g.5184T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.-390T>C MANE Select ENSP00000316244.4:n.-390T>C
ENST00000323865.4:c.-390T>C ENSP00000316244.3:n.-390T>C
ENST00000506598.1:c.-387-3T>C ENSP00000423433.1:n.-387-3T>C
NM_000524.3:c.-390T>C NP_000515.2:n.-390T>C
NM_000524.4:c.-390T>C MANE Select NP_000515.2:n.-390T>C
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