Canonical Allele Identifier: CA120239423

Gene: HTR1A

Linked Data

• dbSNP Id: rs541919096
• gnomAD v3: 5-63959995-A-G
• gnomAD v4: 5-63959995-A-G
• MyVariant Identifiers: chr5:g.63255822A>G (hg19) ; chr5:g.63959995A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.63959995A>G , CM000667.2:g.63959995A>G	GRCh38
NC_000005.9:g.63255822A>G , CM000667.1:g.63255822A>G	GRCh37
NC_000005.8:g.63291578A>G	NCBI36
NG_032816.1:g.7298T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323865.5:c.*456T>C MANE Select	ENSP00000316244.4:n.*456T>C
NM_000524.4:c.*456T>C MANE Select	NP_000515.2:n.*456T>C