Canonical Allele Identifier: CA868684299
Gene: BARX1 HGNC NCBI

Linked Data

dbSNP Id: rs1186111501
gnomAD v3: 9-93953385-A-T
gnomAD v4: 9-93953385-A-T
MyVariant Identifiers: chr9:g.96715667A>T (hg19) chr9:g.93953385A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.93953385A>T , CM000671.2:g.93953385A>T GRCh38
NC_000009.11:g.96715667A>T , CM000671.1:g.96715667A>T GRCh37
NC_000009.10:g.95755488A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000253968.11:c.224-198T>A MANE Select ENSP00000253968.5:n.224-198T>A
ENST00000253968.10:c.224-198T>A ENSP00000253968.5:n.224-198T>A
ENST00000401724.1:c.-437T>A ENSP00000385613.1:n.-437T>A
NM_021570.3:c.224-198T>A NP_067545.3:n.224-198T>A
NM_021570.4:c.224-198T>A MANE Select NP_067545.3:n.224-198T>A
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