Canonical Allele Identifier: CA589466868
Gene: BARX1 HGNC NCBI

Linked Data

dbSNP Id: rs11347798
gnomAD v2: 9-96716220-T-TG
gnomAD v3: 9-93953938-T-TG
gnomAD v4: 9-93953938-T-TG
MyVariant Identifiers: chr9:g.96716221_96716222insG (hg19) chr9:g.96716220_96716221insG (hg19) chr9:g.93953939_93953940insG (hg38) chr9:g.93953938_93953939insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.93953945dup , CM000671.2:g.93953945dup GRCh38
NC_000009.11:g.96716227dup , CM000671.1:g.96716227dup GRCh37
NC_000009.10:g.95756048dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000253968.11:c.224-752dup MANE Select ENSP00000253968.5:n.224-752dup
ENST00000253968.10:c.224-752dup ENSP00000253968.5:n.224-752dup
NM_021570.3:c.224-752dup NP_067545.3:n.224-752dup
NM_021570.4:c.224-752dup MANE Select NP_067545.3:n.224-752dup
Search 100 bp 5'
Search 100 bp 3'