Canonical Allele Identifier: CA10649451
Gene: VSX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 337972
ClinVar RCV Id: RCV000341855
dbSNP Id: rs886056558
gnomAD v4: 20-25082157-G-C
MyVariant Identifiers: chr20:g.25062793G>C (hg19) chr20:g.25082157G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.25082157G>C , CM000682.2:g.25082157G>C GRCh38
NC_000020.10:g.25062793G>C , CM000682.1:g.25062793G>C GRCh37
NC_000020.9:g.25010793G>C NCBI36
NG_008101.1:g.4975C>G
NG_008101.2:g.4975C>G
NG_008101.3:g.5025C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376709.8:c.-61C>G ENSP00000365899.3:n.-61C>G
NM_001256271.1:c.-61C>G NP_001243200.1:n.-61C>G
NM_001256272.1:c.-61C>G NP_001243201.1:n.-61C>G
NM_014588.5:c.-61C>G NP_055403.2:n.-61C>G
NM_199425.2:c.-61C>G NP_955457.1:n.-61C>G
NR_045948.1:n.223C>G
NR_045951.1:n.223C>G
Search 100 bp 5'
Search 100 bp 3'