Canonical Allele Identifier: CA141904030
Gene: HTR1B HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.77463564T>G
GRCh37 chr6:g.78173281T>G
gnomAD v2:
6:78173281 T / G
gnomAD v3:
6:77463564 T / G
gnomAD v4:
chr6-77463564-T-G
Joint Max Group AF 0.00006967 (NFE)
Genomes Max Group AF 0.00003764 (NFE)
Exomes Max Group AF 0.00006862 (NFE)
dbSNP:
130058
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.77463564T>G , CM000668.2:g.77463564T>G GRCh38
NC_000006.11:g.78173281T>G , CM000668.1:g.78173281T>G GRCh37
NC_000006.10:g.78230000T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_000863.2:c.-161A>C NP_000854.1:n.-161A>C
XR_942706.1:n.545-10962T>G
XR_942707.1:n.545-10962T>G
XR_942708.1:n.545-10962T>G
XR_942709.1:n.545-10962T>G
XR_942708.2:n.545-10962T>G
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