Canonical Allele Identifier: CA2709133491
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs2111833759

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63962117G>C , CM000667.2:g.63962117G>C GRCh38
NC_000005.9:g.63257944G>C , CM000667.1:g.63257944G>C GRCh37
NC_000005.8:g.63293700G>C NCBI36
NG_032816.1:g.5176C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.-398C>G MANE Select ENSP00000316244.4:n.-398C>G
ENST00000323865.4:c.-398C>G ENSP00000316244.3:n.-398C>G
ENST00000506598.1:c.-387-11C>G ENSP00000423433.1:n.-387-11C>G
NM_000524.3:c.-398C>G NP_000515.2:n.-398C>G
NM_000524.4:c.-398C>G MANE Select NP_000515.2:n.-398C>G