Canonical Allele Identifier: CA2673998837
Gene: HTR1A HGNC NCBI

Linked Data

gnomAD v4: 5-63960213-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960213C>A , CM000667.2:g.63960213C>A GRCh38
NC_000005.9:g.63256040C>A , CM000667.1:g.63256040C>A GRCh37
NC_000005.8:g.63291796C>A NCBI36
NG_032816.1:g.7080G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.*238G>T MANE Select ENSP00000316244.4:n.*238G>T
NM_000524.3:c.*238G>T NP_000515.2:n.*238G>T
NM_000524.4:c.*238G>T MANE Select NP_000515.2:n.*238G>T