Canonical Allele Identifier: CA560082691
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1383944460
gnomAD v2: 5-63256012-A-G
gnomAD v3: 5-63960185-A-G
gnomAD v4: 5-63960185-A-G
MyVariant Identifiers: chr5:g.63256012A>G (hg19) chr5:g.63960185A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960185A>G , CM000667.2:g.63960185A>G GRCh38
NC_000005.9:g.63256012A>G , CM000667.1:g.63256012A>G GRCh37
NC_000005.8:g.63291768A>G NCBI36
NG_032816.1:g.7108T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000323865.5:c.*266T>C MANE Select ENSP00000316244.4:n.*266T>C
NM_000524.3:c.*266T>C NP_000515.2:n.*266T>C
NM_000524.4:c.*266T>C MANE Select NP_000515.2:n.*266T>C
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