Canonical Allele Identifier: CA2673999412
Gene: HTR1A HGNC NCBI

Linked Data

gnomAD v4: 5-63962107-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63962107C>T , CM000667.2:g.63962107C>T GRCh38
NC_000005.9:g.63257934C>T , CM000667.1:g.63257934C>T GRCh37
NC_000005.8:g.63293690C>T NCBI36
NG_032816.1:g.5186G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.-388G>A MANE Select ENSP00000316244.4:n.-388G>A
ENST00000323865.4:c.-388G>A ENSP00000316244.3:n.-388G>A
ENST00000506598.1:c.-387-1G>A ENSP00000423433.1:n.-387-1G>A
NM_000524.3:c.-388G>A NP_000515.2:n.-388G>A
NM_000524.4:c.-388G>A MANE Select NP_000515.2:n.-388G>A