Canonical Allele Identifier: CA868684601
Gene: BARX1 HGNC NCBI

Linked Data

dbSNP Id: rs1217828543
MyVariant Identifiers: chr9:g.96716447A>C (hg19) chr9:g.93954165A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.93954165A>C , CM000671.2:g.93954165A>C GRCh38
NC_000009.11:g.96716447A>C , CM000671.1:g.96716447A>C GRCh37
NC_000009.10:g.95756268A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000253968.11:c.223+759T>G MANE Select ENSP00000253968.5:n.223+759T>G
ENST00000253968.10:c.223+759T>G ENSP00000253968.5:n.223+759T>G
NM_021570.3:c.223+759T>G NP_067545.3:n.223+759T>G
NM_021570.4:c.223+759T>G MANE Select NP_067545.3:n.223+759T>G
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