Canonical Allele Identifier: CA12273011
Gene: HTR1B HGNC NCBI
dbSNP:
11568817
gnomAD v2:
6:78173382 A / C
gnomAD v3:
6:77463665 A / C
gnomAD v4:
chr6-77463665-A-C
Joint Max Group AF 0.53484621 (MID)
Genomes Max Group AF 0.44547108 (NFE)
Exomes Max Group AF 0.53389972 (MID)
MyVariant.info:
GRCh38 chr6:g.77463665A>C
GRCh37 chr6:g.78173382A>C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.77463665A>C , CM000668.2:g.77463665A>C GRCh38
NC_000006.11:g.78173382A>C , CM000668.1:g.78173382A>C GRCh37
NC_000006.10:g.78230101A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_000863.2:c.-262T>G NP_000854.1:n.-262T>G
XR_942706.1:n.545-10861A>C
XR_942707.1:n.545-10861A>C
XR_942708.1:n.545-10861A>C
XR_942709.1:n.545-10861A>C
XR_942708.2:n.545-10861A>C
Search 100 bp 5'
Search 100 bp 3'