Canonical Allele Identifier: CA1551420590
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs193042484
gnomAD v4: 5-63960286-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960286G>C , CM000667.2:g.63960286G>C GRCh38
NC_000005.9:g.63256113G>C , CM000667.1:g.63256113G>C GRCh37
NC_000005.8:g.63291869G>C NCBI36
NG_032816.1:g.7007C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000323865.5:c.*165C>G MANE Select ENSP00000316244.4:n.*165C>G
NM_000524.3:c.*165C>G NP_000515.2:n.*165C>G
NM_000524.4:c.*165C>G MANE Select NP_000515.2:n.*165C>G
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