Canonical Allele Identifier: CA3280897
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs34118353
gnomAD v2: 5-63256995-G-A
gnomAD v3: 5-63961168-G-A
gnomAD v4: 5-63961168-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63961168G>A , CM000667.2:g.63961168G>A GRCh38
NC_000005.9:g.63256995G>A , CM000667.1:g.63256995G>A GRCh37
NC_000005.8:g.63292751G>A NCBI36
NG_032816.1:g.6125C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.552C>T MANE Select ENSP00000316244.4:p.Pro184=
ENST00000323865.4:c.552C>T ENSP00000316244.3:p.Pro184=
NM_000524.3:c.552C>T NP_000515.2:p.Pro184=
NM_000524.4:c.552C>T MANE Select NP_000515.2:p.Pro184=