Canonical Allele Identifier: CA196446618
Gene: BARX1 HGNC NCBI

Linked Data

dbSNP Id: rs1030424157
gnomAD v3: 9-93953370-C-T
gnomAD v4: 9-93953370-C-T
MyVariant Identifiers: chr9:g.96715652C>T (hg19) chr9:g.93953370C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.93953370C>T , CM000671.2:g.93953370C>T GRCh38
NC_000009.11:g.96715652C>T , CM000671.1:g.96715652C>T GRCh37
NC_000009.10:g.95755473C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000253968.11:c.224-183G>A MANE Select ENSP00000253968.5:n.224-183G>A
ENST00000253968.10:c.224-183G>A ENSP00000253968.5:n.224-183G>A
ENST00000401724.1:c.-422G>A ENSP00000385613.1:n.-422G>A
NM_021570.3:c.224-183G>A NP_067545.3:n.224-183G>A
NM_021570.4:c.224-183G>A MANE Select NP_067545.3:n.224-183G>A
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