Canonical Allele Identifier: CA868684432
Gene: BARX1 HGNC NCBI

Linked Data

dbSNP Id: rs1434386332
MyVariant Identifiers: chr9:g.96716038G>A (hg19) chr9:g.93953756G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.93953756G>A , CM000671.2:g.93953756G>A GRCh38
NC_000009.11:g.96716038G>A , CM000671.1:g.96716038G>A GRCh37
NC_000009.10:g.95755859G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000253968.11:c.224-569C>T MANE Select ENSP00000253968.5:n.224-569C>T
ENST00000253968.10:c.224-569C>T ENSP00000253968.5:n.224-569C>T
NM_021570.3:c.224-569C>T NP_067545.3:n.224-569C>T
NM_021570.4:c.224-569C>T MANE Select NP_067545.3:n.224-569C>T
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