Canonical Allele Identifier: CA196446629
Gene: BARX1 HGNC NCBI

Linked Data

dbSNP Id: rs945989665
gnomAD v3: 9-93953380-G-A
gnomAD v4: 9-93953380-G-A
MyVariant Identifiers: chr9:g.96715662G>A (hg19) chr9:g.93953380G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.93953380G>A , CM000671.2:g.93953380G>A GRCh38
NC_000009.11:g.96715662G>A , CM000671.1:g.96715662G>A GRCh37
NC_000009.10:g.95755483G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000253968.11:c.224-193C>T MANE Select ENSP00000253968.5:n.224-193C>T
ENST00000253968.10:c.224-193C>T ENSP00000253968.5:n.224-193C>T
ENST00000401724.1:c.-432C>T ENSP00000385613.1:n.-432C>T
NM_021570.3:c.224-193C>T NP_067545.3:n.224-193C>T
NM_021570.4:c.224-193C>T MANE Select NP_067545.3:n.224-193C>T
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