Canonical Allele Identifier: CA560082769
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1162205588
gnomAD v2: 5-63257952-A-C
gnomAD v3: 5-63962125-A-C
gnomAD v4: 5-63962125-A-C
MyVariant Identifiers: chr5:g.63257952A>C (hg19) chr5:g.63962125A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63962125A>C , CM000667.2:g.63962125A>C GRCh38
NC_000005.9:g.63257952A>C , CM000667.1:g.63257952A>C GRCh37
NC_000005.8:g.63293708A>C NCBI36
NG_032816.1:g.5168T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.-406T>G MANE Select ENSP00000316244.4:n.-406T>G
ENST00000323865.4:c.-406T>G ENSP00000316244.3:n.-406T>G
ENST00000506598.1:c.-387-19T>G ENSP00000423433.1:n.-387-19T>G
NM_000524.3:c.-406T>G NP_000515.2:n.-406T>G
NM_000524.4:c.-406T>G MANE Select NP_000515.2:n.-406T>G
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