Canonical Allele Identifier: CA120239632
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs977470487
gnomAD v2: 5-63257942-G-A
gnomAD v3: 5-63962115-G-A
gnomAD v4: 5-63962115-G-A
MyVariant Identifiers: chr5:g.63257942G>A (hg19) chr5:g.63962115G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63962115G>A , CM000667.2:g.63962115G>A GRCh38
NC_000005.9:g.63257942G>A , CM000667.1:g.63257942G>A GRCh37
NC_000005.8:g.63293698G>A NCBI36
NG_032816.1:g.5178C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.-396C>T MANE Select ENSP00000316244.4:n.-396C>T
ENST00000323865.4:c.-396C>T ENSP00000316244.3:n.-396C>T
ENST00000506598.1:c.-387-9C>T ENSP00000423433.1:n.-387-9C>T
NM_000524.3:c.-396C>T NP_000515.2:n.-396C>T
NM_000524.4:c.-396C>T MANE Select NP_000515.2:n.-396C>T
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