Canonical Allele Identifier: CA1551420497
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1746393314
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960126C>A , CM000667.2:g.63960126C>A GRCh38
NC_000005.9:g.63255953C>A , CM000667.1:g.63255953C>A GRCh37
NC_000005.8:g.63291709C>A NCBI36
NG_032816.1:g.7167G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.*325G>T MANE Select ENSP00000316244.4:n.*325G>T
NM_000524.3:c.*325G>T NP_000515.2:n.*325G>T
NM_000524.4:c.*325G>T MANE Select NP_000515.2:n.*325G>T
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