Canonical Allele Identifier: CA120239449
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs995706327
gnomAD v3: 5-63960232-T-C
gnomAD v4: 5-63960232-T-C
MyVariant Identifiers: chr5:g.63256059T>C (hg19) chr5:g.63960232T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960232T>C , CM000667.2:g.63960232T>C GRCh38
NC_000005.9:g.63256059T>C , CM000667.1:g.63256059T>C GRCh37
NC_000005.8:g.63291815T>C NCBI36
NG_032816.1:g.7061A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000323865.5:c.*219A>G MANE Select ENSP00000316244.4:n.*219A>G
NM_000524.3:c.*219A>G NP_000515.2:n.*219A>G
NM_000524.4:c.*219A>G MANE Select NP_000515.2:n.*219A>G
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