Canonical Allele Identifier: CA813046899
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1209494533
gnomAD v3: 5-63962203-C-G
gnomAD v4: 5-63962203-C-G
MyVariant Identifiers: chr5:g.63258030C>G (hg19) chr5:g.63962203C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63962203C>G , CM000667.2:g.63962203C>G GRCh38
NC_000005.9:g.63258030C>G , CM000667.1:g.63258030C>G GRCh37
NC_000005.8:g.63293786C>G NCBI36
NG_032816.1:g.5090G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.-484G>C MANE Select ENSP00000316244.4:n.-484G>C
ENST00000506598.1:c.-387-97G>C ENSP00000423433.1:n.-387-97G>C
NM_000524.3:c.-484G>C NP_000515.2:n.-484G>C
NM_000524.4:c.-484G>C MANE Select NP_000515.2:n.-484G>C
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