Canonical Allele Identifier: CA120239444
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs184699261
gnomAD v2: 5-63255968-G-C
gnomAD v3: 5-63960141-G-C
gnomAD v4: 5-63960141-G-C
MyVariant Identifiers: chr5:g.63255968G>C (hg19) chr5:g.63960141G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960141G>C , CM000667.2:g.63960141G>C GRCh38
NC_000005.9:g.63255968G>C , CM000667.1:g.63255968G>C GRCh37
NC_000005.8:g.63291724G>C NCBI36
NG_032816.1:g.7152C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.*310C>G MANE Select ENSP00000316244.4:n.*310C>G
NM_000524.3:c.*310C>G NP_000515.2:n.*310C>G
NM_000524.4:c.*310C>G MANE Select NP_000515.2:n.*310C>G
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