Canonical Allele Identifier: CA120239464
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs900495675
MyVariant Identifiers: chr5:g.63256144T>G (hg19) chr5:g.63960317T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960317T>G , CM000667.2:g.63960317T>G GRCh38
NC_000005.9:g.63256144T>G , CM000667.1:g.63256144T>G GRCh37
NC_000005.8:g.63291900T>G NCBI36
NG_032816.1:g.6976A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000323865.5:c.*134A>C MANE Select ENSP00000316244.4:n.*134A>C
NM_000524.3:c.*134A>C NP_000515.2:n.*134A>C
NM_000524.4:c.*134A>C MANE Select NP_000515.2:n.*134A>C
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