Canonical Allele Identifier: CA2673998832
Gene: HTR1A HGNC NCBI

Linked Data

gnomAD v4: 5-63960209-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960209G>A , CM000667.2:g.63960209G>A GRCh38
NC_000005.9:g.63256036G>A , CM000667.1:g.63256036G>A GRCh37
NC_000005.8:g.63291792G>A NCBI36
NG_032816.1:g.7084C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.*242C>T MANE Select ENSP00000316244.4:n.*242C>T
NM_000524.3:c.*242C>T NP_000515.2:n.*242C>T
NM_000524.4:c.*242C>T MANE Select NP_000515.2:n.*242C>T
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