Canonical Allele Identifier: CA14425187
Gene: SOX9-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs9913711
gnomAD v2: 17-70098161-G-C
gnomAD v3: 17-72102020-G-C
gnomAD v4: 17-72102020-G-C
MyVariant Identifiers: chr17:g.70098161G>C (hg19) chr17:g.72102020G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72102020G>C , CM000679.2:g.72102020G>C GRCh38
NC_000017.10:g.70098161G>C , CM000679.1:g.70098161G>C GRCh37
NC_000017.9:g.67609756G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103737.1:n.32-17992C>G
NR_103738.1:n.358+12186C>G
Search 100 bp 5'
Search 100 bp 3'