Canonical Allele Identifier: CA1551420544
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1746395522
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960207T>C , CM000667.2:g.63960207T>C GRCh38
NC_000005.9:g.63256034T>C , CM000667.1:g.63256034T>C GRCh37
NC_000005.8:g.63291790T>C NCBI36
NG_032816.1:g.7086A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.*244A>G MANE Select ENSP00000316244.4:n.*244A>G
NM_000524.3:c.*244A>G NP_000515.2:n.*244A>G
NM_000524.4:c.*244A>G MANE Select NP_000515.2:n.*244A>G
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