Canonical Allele Identifier: CA813042912
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1430584034
gnomAD v3: 5-63960158-GCAATTA-G
gnomAD v4: 5-63960158-GCAATTA-G
MyVariant Identifiers: chr5:g.63255986_63255991del (hg19) chr5:g.63960159_63960164del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960160_63960165del , CM000667.2:g.63960160_63960165del GRCh38
NC_000005.9:g.63255987_63255992del , CM000667.1:g.63255987_63255992del GRCh37
NC_000005.8:g.63291743_63291748del NCBI36
NG_032816.1:g.7129_7134del

Transcript Alleles

HGVS Amino-acid Change
ENST00000323865.5:c.*287_*292del MANE Select ENSP00000316244.4:n.*287_*292del
NM_000524.3:c.*287_*292del NP_000515.2:n.*287_*292del
NM_000524.4:c.*287_*292del MANE Select NP_000515.2:n.*287_*292del
Search 100 bp 5'
Search 100 bp 3'