Canonical Allele Identifier: CA2673999528
Gene: HTR1A HGNC NCBI

Linked Data

gnomAD v4: 5-63962204-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63962204T>G , CM000667.2:g.63962204T>G GRCh38
NC_000005.9:g.63258031T>G , CM000667.1:g.63258031T>G GRCh37
NC_000005.8:g.63293787T>G NCBI36
NG_032816.1:g.5089A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.-485A>C MANE Select ENSP00000316244.4:n.-485A>C
ENST00000506598.1:c.-387-98A>C ENSP00000423433.1:n.-387-98A>C
NM_000524.3:c.-485A>C NP_000515.2:n.-485A>C
NM_000524.4:c.-485A>C MANE Select NP_000515.2:n.-485A>C