Canonical Allele Identifier: CA868684592
Gene: BARX1 HGNC NCBI

Linked Data

dbSNP Id: rs1233320047
MyVariant Identifiers: chr9:g.96716415C>T (hg19) chr9:g.93954133C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.93954133C>T , CM000671.2:g.93954133C>T GRCh38
NC_000009.11:g.96716415C>T , CM000671.1:g.96716415C>T GRCh37
NC_000009.10:g.95756236C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000253968.11:c.223+791G>A MANE Select ENSP00000253968.5:n.223+791G>A
ENST00000253968.10:c.223+791G>A ENSP00000253968.5:n.223+791G>A
NM_021570.3:c.223+791G>A NP_067545.3:n.223+791G>A
NM_021570.4:c.223+791G>A MANE Select NP_067545.3:n.223+791G>A
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