Canonical Allele Identifier: CA1551420588
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1746397557
gnomAD v4: 5-63960284-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960284C>G , CM000667.2:g.63960284C>G GRCh38
NC_000005.9:g.63256111C>G , CM000667.1:g.63256111C>G GRCh37
NC_000005.8:g.63291867C>G NCBI36
NG_032816.1:g.7009G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000323865.5:c.*167G>C MANE Select ENSP00000316244.4:n.*167G>C
NM_000524.3:c.*167G>C NP_000515.2:n.*167G>C
NM_000524.4:c.*167G>C MANE Select NP_000515.2:n.*167G>C
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