Canonical Allele Identifier: CA2673999519
Gene: HTR1A HGNC NCBI

Linked Data

gnomAD v4: 5-63962200-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63962200T>C , CM000667.2:g.63962200T>C GRCh38
NC_000005.9:g.63258027T>C , CM000667.1:g.63258027T>C GRCh37
NC_000005.8:g.63293783T>C NCBI36
NG_032816.1:g.5093A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.-481A>G MANE Select ENSP00000316244.4:n.-481A>G
ENST00000506598.1:c.-387-94A>G ENSP00000423433.1:n.-387-94A>G
NM_000524.3:c.-481A>G NP_000515.2:n.-481A>G
NM_000524.4:c.-481A>G MANE Select NP_000515.2:n.-481A>G
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