Canonical Allele Identifier: CA2673999536
Gene: HTR1A HGNC NCBI

Linked Data

gnomAD v4: 5-63962208-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63962208T>C , CM000667.2:g.63962208T>C GRCh38
NC_000005.9:g.63258035T>C , CM000667.1:g.63258035T>C GRCh37
NC_000005.8:g.63293791T>C NCBI36
NG_032816.1:g.5085A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.-489A>G MANE Select ENSP00000316244.4:n.-489A>G
ENST00000506598.1:c.-387-102A>G ENSP00000423433.1:n.-387-102A>G
NM_000524.3:c.-489A>G NP_000515.2:n.-489A>G
NM_000524.4:c.-489A>G MANE Select NP_000515.2:n.-489A>G