Canonical Allele Identifier: CA11676953
Gene: STX18-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr4:g.4702287C>T
GRCh37 chr4:g.4704014C>T
gnomAD v2:
4:4704014 C / T
gnomAD v3:
4:4702287 C / T
gnomAD v4:
chr4-4702287-C-T
Joint Max Group AF 0.72444026 (AFR)
Genomes Max Group AF 0.72444026 (AFR)
dbSNP:
4476553
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4702287C>T , CM000666.2:g.4702287C>T GRCh38
NC_000004.11:g.4704014C>T , CM000666.1:g.4704014C>T GRCh37
NC_000004.10:g.4754915C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037888.1:n.819-3386C>T
Search 100 bp 5'
Search 100 bp 3'