Canonical Allele Identifier: CA120239641
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs921557859
gnomAD v4: 5-63962207-C-T
MyVariant Identifiers: chr5:g.63258034C>T (hg19) chr5:g.63962207C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63962207C>T , CM000667.2:g.63962207C>T GRCh38
NC_000005.9:g.63258034C>T , CM000667.1:g.63258034C>T GRCh37
NC_000005.8:g.63293790C>T NCBI36
NG_032816.1:g.5086G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.-488G>A MANE Select ENSP00000316244.4:n.-488G>A
ENST00000506598.1:c.-387-101G>A ENSP00000423433.1:n.-387-101G>A
NM_000524.3:c.-488G>A NP_000515.2:n.-488G>A
NM_000524.4:c.-488G>A MANE Select NP_000515.2:n.-488G>A
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