Canonical Allele Identifier: CA813042965
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1407251351
MyVariant Identifiers: chr5:g.63256077C>T (hg19) chr5:g.63960250C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960250C>T , CM000667.2:g.63960250C>T GRCh38
NC_000005.9:g.63256077C>T , CM000667.1:g.63256077C>T GRCh37
NC_000005.8:g.63291833C>T NCBI36
NG_032816.1:g.7043G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000323865.5:c.*201G>A MANE Select ENSP00000316244.4:n.*201G>A
NM_000524.3:c.*201G>A NP_000515.2:n.*201G>A
NM_000524.4:c.*201G>A MANE Select NP_000515.2:n.*201G>A
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